Bristol-Myers Squibb in Uxbridge is seeking an Associate Director of Clinical Data Management to lead critical data management tasks in clinical trials. The successful candidate will own complex clinical programmes, setting and adhering to high data standards while mentoring junior staff. The role includes collaboration with cross-functional teams to ensure data integrity and quality oversight, making it essential in the development of life-changing medicines. This position requires a Bachelor's degree in a relevant field with 7+ years of experience in the biopharma industry.
23/07/2026
Full time
Bristol-Myers Squibb in Uxbridge is seeking an Associate Director of Clinical Data Management to lead critical data management tasks in clinical trials. The successful candidate will own complex clinical programmes, setting and adhering to high data standards while mentoring junior staff. The role includes collaboration with cross-functional teams to ensure data integrity and quality oversight, making it essential in the development of life-changing medicines. This position requires a Bachelor's degree in a relevant field with 7+ years of experience in the biopharma industry.
Associate Director, Clinical Data ManagementUxbridge - GBFind out how well you match with this job Working with Us Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: What if your next role helped change the course of a patient's life? At Bristol Myers Squibb, that's not a motivational tagline - it's the reality of what you'd be doing every single day.We're looking for an Associate Director of Clinical Data Management to join us at our Uxbridge site. This is a role where your expertise doesn't just support a clinical trial - it drives it . The data you champion, the standards you set, and the teams you lead are what ultimately move life-changing medicines from the lab to the people who need them most.If you're someone who finds purpose in precision, thrives in complexity, and wants to lead - not just participate - then read on. This is your chance to lead, not just deliver You'll step into a genuine leadership position at the heart of BMS's R&D pipeline - one of the most promising in the industry. You won't be managing data in isolation. You'll be the person that cross-functional teams turn to, the voice of data management in study teams and at the executive table, and the expert who sets the standard others follow.In practical terms, that means: Owning end-to-end data management across one or more complex, high-stakes clinical development programmes - with the autonomy to shape how they run Setting programme-level data standards in partnership with global teams, leaving a legacy that outlasts any single trial Leading Data Quality Review meetings , ensuring the integrity and completeness of trial data that underpins regulatory submissions worldwide Mentoring junior Data Management Leads , helping the next generation of talent grow - and growing your own leadership reputation in the process Representing Data Management on cross-functional and regulatory submission teams , giving you visibility and influence across the full breadth of the organisationThis isn't a role where you wait for direction. You are the direction. The problems you'll solve are genuinely hard and that's the point Clinical trials are complex. Multi-vendor. Multi-system. High-pressure. And the margin for error is slim when patient safety and regulatory approval are on the line.You'll be working with EDC systems (Medidata RAVE), integrating data from eCOA, External Data, and Safety Gateway platforms, and overseeing third-party vendors and CROs to ensure everything runs to the agreed SLA. You'll author and review critical study documentation - from Data Quality Management Plans to eCRF Completion Guidelines - and you'll lead or support Health Authority inspections and audits when it really counts. What does that mean for you? You'll build a track record that is visible, verifiable, and genuinely impressive. The kind of experience that doesn't just look good on a CV - it shapes who you are as a leader in this industry. You'll be part of something bigger than any single study BMS is a company that takes its mission seriously: to discover, develop and deliver innovative medicines that help patients prevail over serious diseases . That mission runs through everything here, and in this role, you'll feel it.You'll also have the opportunity to drive continuous improvement - evaluating new technologies, contributing to functional SOPs, and supporting change management initiatives that have broad impact across the organisation. If you've ever had ideas about how clinical data management could work better, this is the environment where you can actually make those ideas happen.And with just 5-10% travel to industry conferences, investigator meetings, and regulatory inspections, you'll have the balance to do deep, meaningful work - while staying connected to the wider clinical community. What you'll bring 7+ years of experience in biopharma or CRO environments, with at least 3 years in a study or programme leadership role Strong working knowledge of FDA/ICH guidelines and industry data management practices Hands-on experience with EDC systems , ideally Medidata RAVE A sharp eye for metrics, reporting, and quality oversight The communication skills to hold a room - whether that's with a junior team member or a senior regulatory authority A Bachelor's degree in life sciences, data science, or statistics (advanced degree a bonus, not a barrier) If you come across a role that intrigues you but doesn't perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career. Uniquely Interesting Work, Life-changing Careers With a single vision as inspiring as "Transforming patients' lives through scienceTM ", every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues. On-site Protocol BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function. Supporting People with Disabilities BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to . Visit to access our complete Equal Employment Opportunity statement.Bristol Myers Squibb is Disability Confident - EmployerA UK Government scheme Candidate Rights BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area. Data Protection We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at . Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley.R : Associate Director, Clinical Data Management
23/07/2026
Full time
Associate Director, Clinical Data ManagementUxbridge - GBFind out how well you match with this job Working with Us Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: What if your next role helped change the course of a patient's life? At Bristol Myers Squibb, that's not a motivational tagline - it's the reality of what you'd be doing every single day.We're looking for an Associate Director of Clinical Data Management to join us at our Uxbridge site. This is a role where your expertise doesn't just support a clinical trial - it drives it . The data you champion, the standards you set, and the teams you lead are what ultimately move life-changing medicines from the lab to the people who need them most.If you're someone who finds purpose in precision, thrives in complexity, and wants to lead - not just participate - then read on. This is your chance to lead, not just deliver You'll step into a genuine leadership position at the heart of BMS's R&D pipeline - one of the most promising in the industry. You won't be managing data in isolation. You'll be the person that cross-functional teams turn to, the voice of data management in study teams and at the executive table, and the expert who sets the standard others follow.In practical terms, that means: Owning end-to-end data management across one or more complex, high-stakes clinical development programmes - with the autonomy to shape how they run Setting programme-level data standards in partnership with global teams, leaving a legacy that outlasts any single trial Leading Data Quality Review meetings , ensuring the integrity and completeness of trial data that underpins regulatory submissions worldwide Mentoring junior Data Management Leads , helping the next generation of talent grow - and growing your own leadership reputation in the process Representing Data Management on cross-functional and regulatory submission teams , giving you visibility and influence across the full breadth of the organisationThis isn't a role where you wait for direction. You are the direction. The problems you'll solve are genuinely hard and that's the point Clinical trials are complex. Multi-vendor. Multi-system. High-pressure. And the margin for error is slim when patient safety and regulatory approval are on the line.You'll be working with EDC systems (Medidata RAVE), integrating data from eCOA, External Data, and Safety Gateway platforms, and overseeing third-party vendors and CROs to ensure everything runs to the agreed SLA. You'll author and review critical study documentation - from Data Quality Management Plans to eCRF Completion Guidelines - and you'll lead or support Health Authority inspections and audits when it really counts. What does that mean for you? You'll build a track record that is visible, verifiable, and genuinely impressive. The kind of experience that doesn't just look good on a CV - it shapes who you are as a leader in this industry. You'll be part of something bigger than any single study BMS is a company that takes its mission seriously: to discover, develop and deliver innovative medicines that help patients prevail over serious diseases . That mission runs through everything here, and in this role, you'll feel it.You'll also have the opportunity to drive continuous improvement - evaluating new technologies, contributing to functional SOPs, and supporting change management initiatives that have broad impact across the organisation. If you've ever had ideas about how clinical data management could work better, this is the environment where you can actually make those ideas happen.And with just 5-10% travel to industry conferences, investigator meetings, and regulatory inspections, you'll have the balance to do deep, meaningful work - while staying connected to the wider clinical community. What you'll bring 7+ years of experience in biopharma or CRO environments, with at least 3 years in a study or programme leadership role Strong working knowledge of FDA/ICH guidelines and industry data management practices Hands-on experience with EDC systems , ideally Medidata RAVE A sharp eye for metrics, reporting, and quality oversight The communication skills to hold a room - whether that's with a junior team member or a senior regulatory authority A Bachelor's degree in life sciences, data science, or statistics (advanced degree a bonus, not a barrier) If you come across a role that intrigues you but doesn't perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career. Uniquely Interesting Work, Life-changing Careers With a single vision as inspiring as "Transforming patients' lives through scienceTM ", every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues. On-site Protocol BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function. Supporting People with Disabilities BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to . Visit to access our complete Equal Employment Opportunity statement.Bristol Myers Squibb is Disability Confident - EmployerA UK Government scheme Candidate Rights BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area. Data Protection We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at . Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley.R : Associate Director, Clinical Data Management
Bristol Myers Squibb is seeking a Senior Manager of Clinical Data Management to lead end-to-end data management for high-impact trials. You will be the go-to for internal teams and external partners, setting data quality standards and ensuring timely, audit-ready datasets. The role requires 5+ years in clinical data management, hands-on EDC experience (Medidata RAVE a strong plus), and collaboration across regulatory, operations, and R&D.
16/07/2026
Full time
Bristol Myers Squibb is seeking a Senior Manager of Clinical Data Management to lead end-to-end data management for high-impact trials. You will be the go-to for internal teams and external partners, setting data quality standards and ensuring timely, audit-ready datasets. The role requires 5+ years in clinical data management, hands-on EDC experience (Medidata RAVE a strong plus), and collaboration across regulatory, operations, and R&D.
Working with UsChallenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: you ready to do the work of your career?At Bristol Myers Squibb, we believe that the right data, in the right hands, at the right time can change everything. Every clinical trial we run brings us closer to a treatment that could transform or save a patient's life.As our Senior Manager of Clinical Data Management, you'll be the person who makes that possible.This isn't just a data role. It's a leadership position at the heart of our R&D pipeline; where your decisions, your standards, and your expertise directly shape the speed and quality of life-changing medicines reaching patients worldwide.What You'll Be DoingLeading Where It Matters MostYou'll take the wheel on end-to-end clinical data management for some of our most complex and impactful trials. That means being the go-to person for both internal teams and external partners, the one who sets the bar for data quality and makes sure everyone clears it.Drive data collection strategy across one or more complex clinical development projects, aligning cross-functional teams around clear, high-quality standardsOwn the full data management lifecycle, from planning and collection through to clean, submission-ready datasets delivered on timeShape the systems that power our trials, leading requirements gathering for EDC platforms and collaborating with partners across eCOA, External Data, and Safety GatewayChair Data Quality Review meetings to keep trial data current, complete, and audit-ready at every stageAuthor and review key study documents, Data Quality Management Plans, Data Validation Plans, eCRF Completion Guidelines and more, ensuring consistency and compliance across the boardMentoring the Next GenerationOne of the most rewarding parts of this role? You'll coach and guide junior Data Management Leads, helping them grow while raising the overall capability of the team. Your expertise becomes their foundation.Representing DM at the Highest LevelYou'll sit at the table for cross-functional project teams and regulatory submission teams, and you'll be a key player during Health Authority inspections and audits. This is a role where your voice carries real weight.Vendor Oversight & PartnershipsWhether working with FSPs, CROs, or third-party vendors, you'll be the quality compass; monitoring deliverables, managing data currency throughout the trial, and holding partners accountable to SLAs that protect the integrity of our work.Driving Continuous ImprovementYou'll contribute meaningfully to how we evolve as an organisation - supporting CAPA implementation and bringing fresh thinking to continuous improvement initiatives within Clinical Data Management.What's In It For YouMeaningful impact, your work directly supports the development of medicines that matter to millions of patients globallyCareer elevation, step into a senior leadership role with visibility across R&D and a clear path toward Director-level progressionCross-functional influence, build relationships across clinical operations, regulatory, biostatistics, and beyondIndustry exposure, travel to conferences, investigator meetings, and regulatory engagements (approximately 5-10% travel) to stay at the forefront of your fieldIntellectual challenge, work with cutting-edge data collection technologies and emerging industry trends that keep your skills sharp and future-proofWhat You'll BringA Bachelor's Degree (advanced degree preferred) and at least 5 years of relevant industry experienceA strong command of clinical drug development processes, FDA/ICH guidelines, and data management best practicesHands-on experience with EDC systems; Medidata RAVE experience is a strong plusProven project management skills, with a PMP certification considered a bonusThe ability to translate complex data into clear insights through metrics analysis and reportingOutstanding communication skills, whether you're presenting to senior leadership or collaborating with a vendor team, you know how to land the messageFamiliarity with submission requirements including NDA, BLA, and MAA processesReady to Apply?If you're someone who takes pride in doing rigorous work and inspiring others to do the same, someone who sees clinical data not just as numbers, but as the foundation of scientific truth, we'd love to hear from you.Join BMS. Transform patients' lives. Build your own. you come across a role that intrigues you but doesn't perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.Uniquely Interesting Work, Life-changing CareersWith a single vision as inspiring as "Transforming patients' lives through science ", every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.On-site ProtocolBMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.Supporting People with DisabilitiesBMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to . Visit to access our complete Equal Employment Opportunity statement.Bristol Myers Squibb is Disability Confident - EmployerA UK Government schemeCandidate RightsBMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.Data ProtectionWe will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at . Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley.R : Senior Manager, Clinical Data Management
16/07/2026
Full time
Working with UsChallenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: you ready to do the work of your career?At Bristol Myers Squibb, we believe that the right data, in the right hands, at the right time can change everything. Every clinical trial we run brings us closer to a treatment that could transform or save a patient's life.As our Senior Manager of Clinical Data Management, you'll be the person who makes that possible.This isn't just a data role. It's a leadership position at the heart of our R&D pipeline; where your decisions, your standards, and your expertise directly shape the speed and quality of life-changing medicines reaching patients worldwide.What You'll Be DoingLeading Where It Matters MostYou'll take the wheel on end-to-end clinical data management for some of our most complex and impactful trials. That means being the go-to person for both internal teams and external partners, the one who sets the bar for data quality and makes sure everyone clears it.Drive data collection strategy across one or more complex clinical development projects, aligning cross-functional teams around clear, high-quality standardsOwn the full data management lifecycle, from planning and collection through to clean, submission-ready datasets delivered on timeShape the systems that power our trials, leading requirements gathering for EDC platforms and collaborating with partners across eCOA, External Data, and Safety GatewayChair Data Quality Review meetings to keep trial data current, complete, and audit-ready at every stageAuthor and review key study documents, Data Quality Management Plans, Data Validation Plans, eCRF Completion Guidelines and more, ensuring consistency and compliance across the boardMentoring the Next GenerationOne of the most rewarding parts of this role? You'll coach and guide junior Data Management Leads, helping them grow while raising the overall capability of the team. Your expertise becomes their foundation.Representing DM at the Highest LevelYou'll sit at the table for cross-functional project teams and regulatory submission teams, and you'll be a key player during Health Authority inspections and audits. This is a role where your voice carries real weight.Vendor Oversight & PartnershipsWhether working with FSPs, CROs, or third-party vendors, you'll be the quality compass; monitoring deliverables, managing data currency throughout the trial, and holding partners accountable to SLAs that protect the integrity of our work.Driving Continuous ImprovementYou'll contribute meaningfully to how we evolve as an organisation - supporting CAPA implementation and bringing fresh thinking to continuous improvement initiatives within Clinical Data Management.What's In It For YouMeaningful impact, your work directly supports the development of medicines that matter to millions of patients globallyCareer elevation, step into a senior leadership role with visibility across R&D and a clear path toward Director-level progressionCross-functional influence, build relationships across clinical operations, regulatory, biostatistics, and beyondIndustry exposure, travel to conferences, investigator meetings, and regulatory engagements (approximately 5-10% travel) to stay at the forefront of your fieldIntellectual challenge, work with cutting-edge data collection technologies and emerging industry trends that keep your skills sharp and future-proofWhat You'll BringA Bachelor's Degree (advanced degree preferred) and at least 5 years of relevant industry experienceA strong command of clinical drug development processes, FDA/ICH guidelines, and data management best practicesHands-on experience with EDC systems; Medidata RAVE experience is a strong plusProven project management skills, with a PMP certification considered a bonusThe ability to translate complex data into clear insights through metrics analysis and reportingOutstanding communication skills, whether you're presenting to senior leadership or collaborating with a vendor team, you know how to land the messageFamiliarity with submission requirements including NDA, BLA, and MAA processesReady to Apply?If you're someone who takes pride in doing rigorous work and inspiring others to do the same, someone who sees clinical data not just as numbers, but as the foundation of scientific truth, we'd love to hear from you.Join BMS. Transform patients' lives. Build your own. you come across a role that intrigues you but doesn't perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.Uniquely Interesting Work, Life-changing CareersWith a single vision as inspiring as "Transforming patients' lives through science ", every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.On-site ProtocolBMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.Supporting People with DisabilitiesBMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to . Visit to access our complete Equal Employment Opportunity statement.Bristol Myers Squibb is Disability Confident - EmployerA UK Government schemeCandidate RightsBMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.Data ProtectionWe will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at . Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley.R : Senior Manager, Clinical Data Management
Bristol Myers Squibb UK is seeking a Senior Manager, Patient Safety Science to shape safety strategies and ensure robust pharmacovigilance across the product lifecycle. You will collaborate with Medical Safety Assessment Physicians and Safety Management Teams to own signal detection and safety data reviews. The role emphasizes cross-functional leadership, use of AI/digital platforms to enhance safety workflows, and development of risk management plans, with hybrid work arrangements in the UK.
12/07/2026
Full time
Bristol Myers Squibb UK is seeking a Senior Manager, Patient Safety Science to shape safety strategies and ensure robust pharmacovigilance across the product lifecycle. You will collaborate with Medical Safety Assessment Physicians and Safety Management Teams to own signal detection and safety data reviews. The role emphasizes cross-functional leadership, use of AI/digital platforms to enhance safety workflows, and development of risk management plans, with hybrid work arrangements in the UK.
Bristol-Myers Squibb is looking for a Senior Statistical Programmer in Uxbridge to transform clinical data into life-changing decisions. The role involves writing and validating SAS programs, contributing to electronic submissions, and leading programming assignments with autonomy. Ideal candidates will have a Bachelor's degree in a relevant field and experience in statistical programming. You will collaborate closely with clinical teams to enhance efficiency in the drug development process.
06/07/2026
Full time
Bristol-Myers Squibb is looking for a Senior Statistical Programmer in Uxbridge to transform clinical data into life-changing decisions. The role involves writing and validating SAS programs, contributing to electronic submissions, and leading programming assignments with autonomy. Ideal candidates will have a Bachelor's degree in a relevant field and experience in statistical programming. You will collaborate closely with clinical teams to enhance efficiency in the drug development process.
Senior Statistical ProgrammerUxbridge - GBFind out how well you match with this job Working with Us Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: Are you ready to turn clinical data into life-changing decisions? At Bristol Myers Squibb , we believe that behind every dataset, every line of code, and every submission package, there's a patient waiting for a better option. As our Senior Statistical Programmer , you are one of the people who makes that happen.This isn't a role where your work disappears into a black box. Here, your programming expertise directly shapes how new medicines are developed, reviewed by regulators, and ultimately approved for patients around the world. That's a pretty remarkable thing to be part of. What you'll actually be doing You'll be a key technical voice within our Global Biometrics & Data Sciences (GBDS) function, working closely with cross-functional clinical teams, collaborating with external vendors, and owning your programming workload with real autonomy.This is a focused individual contributor role - no line management responsibilities - so you can put your energy exactly where it matters most: delivering high-quality, high-impact programming work. Day to day, that looks like: Writing and validating SAS programs to generate derived analysis datasets and clinical Tables, Figures, and Listings (TFLs) - work that feeds directly into regulatory decision-making Contributing to electronic submission preparation (think NDA, BLA, MAA ) - real regulatory milestones that mark pivotal moments in a medicine's journey Reviewing and shaping key planning documents like Statistical Analysis Plans (SAPs) and Data Presentation Plans , ensuring clarity and completeness before programming work begins - your input genuinely steers project direction Partnering with vendors on programming standards, specifications, and file transfers , building the kind of collaborative relationships that make complex programmes run smoothly Independently leading programming assignments across multiple projects with minimal supervision - you'll have real ownership and the trust to match it Spotting opportunities to improve efficiency and consistency across GBDS, contributing to initiatives that make the whole team better What you bring to the table We're looking for someone with a solid foundation and the drive to apply it meaningfully. Here's what we need: Education & Background A Bachelor's degree in Statistics, Biostatistics, Mathematics, Computer Science, or Life Sciences Demonstrated industry experience in statistical programming Core Skills & Knowledge Strong, proven proficiency in SAS for producing derived analysis datasets and TFLs In-depth understanding of clinical data structures , including CDISC standards (SDTM, ADaM) and relational databases Hands-on experience with upstream data handling - multiple data forms, eDC , workflow, and SDTM Ability to deliver downstream outputs including ADaM datasets, Data Definition Tables, and e-submission packages Confidence with tools like MS Office, XML and Pinnacle 21 A solid grasp of regulatory, industry, and technology standards - you understand why the rules exist, not just what they are Familiarity with statistical terminology, clinical trial methodology, medical terminology, and protocol designs A genuine team player - you communicate well, build bridges across functions, and make the people around you more effective It'd be a bonus if you also have Deep experience supporting global regulatory filings (NDA, BLA, MAA) within pharma clinical development Broad knowledge of the end-to-end drug development process and global regulatory frameworks Experience with R or other statistical programming languages Familiarity with the Linux operating system Why this role, why BMS, why now? Here, your skills aren't just technically valued - they're mission critical . You'll work in an environment that respects your expertise, gives you the autonomy to lead your own work, and connects your daily output to outcomes that genuinely matter. You'll gain: Exposure to the full clinical development lifecycle , from data collection through to regulatory submission The chance to work with industry-leading standards and technologies in a global biometrics function A culture that actively encourages you to identify improvements and champion change - your ideas won't gather dust here Collaboration with talented, purpose-driven colleagues across global cross-functional teams If you come across a role that intrigues you but doesn't perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career. Uniquely Interesting Work, Life-changing Careers With a single vision as inspiring as "Transforming patients' lives through scienceTM ", every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues. On-site Protocol BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function. Supporting People with Disabilities BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to . Visit to access our complete Equal Employment Opportunity statement.Bristol Myers Squibb is Disability Confident - EmployerA UK Government scheme Candidate Rights BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area. Data Protection We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at . Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley.R : Senior Statistical Programmer
06/07/2026
Full time
Senior Statistical ProgrammerUxbridge - GBFind out how well you match with this job Working with Us Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: Are you ready to turn clinical data into life-changing decisions? At Bristol Myers Squibb , we believe that behind every dataset, every line of code, and every submission package, there's a patient waiting for a better option. As our Senior Statistical Programmer , you are one of the people who makes that happen.This isn't a role where your work disappears into a black box. Here, your programming expertise directly shapes how new medicines are developed, reviewed by regulators, and ultimately approved for patients around the world. That's a pretty remarkable thing to be part of. What you'll actually be doing You'll be a key technical voice within our Global Biometrics & Data Sciences (GBDS) function, working closely with cross-functional clinical teams, collaborating with external vendors, and owning your programming workload with real autonomy.This is a focused individual contributor role - no line management responsibilities - so you can put your energy exactly where it matters most: delivering high-quality, high-impact programming work. Day to day, that looks like: Writing and validating SAS programs to generate derived analysis datasets and clinical Tables, Figures, and Listings (TFLs) - work that feeds directly into regulatory decision-making Contributing to electronic submission preparation (think NDA, BLA, MAA ) - real regulatory milestones that mark pivotal moments in a medicine's journey Reviewing and shaping key planning documents like Statistical Analysis Plans (SAPs) and Data Presentation Plans , ensuring clarity and completeness before programming work begins - your input genuinely steers project direction Partnering with vendors on programming standards, specifications, and file transfers , building the kind of collaborative relationships that make complex programmes run smoothly Independently leading programming assignments across multiple projects with minimal supervision - you'll have real ownership and the trust to match it Spotting opportunities to improve efficiency and consistency across GBDS, contributing to initiatives that make the whole team better What you bring to the table We're looking for someone with a solid foundation and the drive to apply it meaningfully. Here's what we need: Education & Background A Bachelor's degree in Statistics, Biostatistics, Mathematics, Computer Science, or Life Sciences Demonstrated industry experience in statistical programming Core Skills & Knowledge Strong, proven proficiency in SAS for producing derived analysis datasets and TFLs In-depth understanding of clinical data structures , including CDISC standards (SDTM, ADaM) and relational databases Hands-on experience with upstream data handling - multiple data forms, eDC , workflow, and SDTM Ability to deliver downstream outputs including ADaM datasets, Data Definition Tables, and e-submission packages Confidence with tools like MS Office, XML and Pinnacle 21 A solid grasp of regulatory, industry, and technology standards - you understand why the rules exist, not just what they are Familiarity with statistical terminology, clinical trial methodology, medical terminology, and protocol designs A genuine team player - you communicate well, build bridges across functions, and make the people around you more effective It'd be a bonus if you also have Deep experience supporting global regulatory filings (NDA, BLA, MAA) within pharma clinical development Broad knowledge of the end-to-end drug development process and global regulatory frameworks Experience with R or other statistical programming languages Familiarity with the Linux operating system Why this role, why BMS, why now? Here, your skills aren't just technically valued - they're mission critical . You'll work in an environment that respects your expertise, gives you the autonomy to lead your own work, and connects your daily output to outcomes that genuinely matter. You'll gain: Exposure to the full clinical development lifecycle , from data collection through to regulatory submission The chance to work with industry-leading standards and technologies in a global biometrics function A culture that actively encourages you to identify improvements and champion change - your ideas won't gather dust here Collaboration with talented, purpose-driven colleagues across global cross-functional teams If you come across a role that intrigues you but doesn't perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career. Uniquely Interesting Work, Life-changing Careers With a single vision as inspiring as "Transforming patients' lives through scienceTM ", every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues. On-site Protocol BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function. Supporting People with Disabilities BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to . Visit to access our complete Equal Employment Opportunity statement.Bristol Myers Squibb is Disability Confident - EmployerA UK Government scheme Candidate Rights BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area. Data Protection We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at . Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley.R : Senior Statistical Programmer
Bristol-Myers Squibb is seeking a Senior Manager, Data Science, in Uxbridge, UK. This pivotal role involves applying sophisticated computational methods and statistical analyses to enhance drug development using complex data types. The ideal candidate will have a PhD or Master's in a quantitative field, expertise in machine learning, and proficiency in Python and R. Join a team committed to transforming patients' lives through innovative science and analytics.
05/07/2026
Full time
Bristol-Myers Squibb is seeking a Senior Manager, Data Science, in Uxbridge, UK. This pivotal role involves applying sophisticated computational methods and statistical analyses to enhance drug development using complex data types. The ideal candidate will have a PhD or Master's in a quantitative field, expertise in machine learning, and proficiency in Python and R. Join a team committed to transforming patients' lives through innovative science and analytics.
Bristol-Myers Squibb is searching for an Associate Director, Data Science to join its team in Uxbridge, UK. The role focuses on harnessing advanced analytics and machine learning techniques to inform drug development strategies across clinical trials. Ideal candidates hold a relevant PhD with 6+ years of industry experience, demonstrating a strong proficiency in data science methodologies and statistical analysis. They will engage in aspects of data quality frameworks and lead a team of data scientists in a hybrid work setting.
03/07/2026
Full time
Bristol-Myers Squibb is searching for an Associate Director, Data Science to join its team in Uxbridge, UK. The role focuses on harnessing advanced analytics and machine learning techniques to inform drug development strategies across clinical trials. Ideal candidates hold a relevant PhD with 6+ years of industry experience, demonstrating a strong proficiency in data science methodologies and statistical analysis. They will engage in aspects of data quality frameworks and lead a team of data scientists in a hybrid work setting.
Senior Manager, Clinical Data ManagementUxbridge - GBFind out how well you match with this job Working with Us Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: Are you ready to do the work of your career? At Bristol Myers Squibb, we believe that the right data, in the right hands, at the right time can change everything. Every clinical trial we run brings us closer to a treatment that could transform or save a patient's life.As our Senior Manager of Clinical Data Management, you'll be the person who makes that possible. This isn't just a data role. It's a leadership position at the heart of our R&D pipeline; where your decisions, your standards, and your expertise directly shape the speed and quality of life-changing medicines reaching patients worldwide. What You'll Be Doing Leading Where It Matters Most You'll take the wheel on end-to-end clinical data management for some of our most complex and impactful trials. That means being the go-to person for both internal teams and external partners, the one who sets the bar for data quality and makes sure everyone clears it. Drive data collection strategy across one or more complex clinical development projects, aligning cross-functional teams around clear, high-quality standards Own the full data management lifecycle, from planning and collection through to clean, submission-ready datasets delivered on time Shape the systems that power our trials, leading requirements gathering for EDC platforms and collaborating with partners across eCOA, External Data, and Safety Gateway Chair Data Quality Review meetings to keep trial data current, complete, and audit-ready at every stage Author and review key study documents, Data Quality Management Plans, Data Validation Plans, eCRF Completion Guidelines and more, ensuring consistency and compliance across the board Mentoring the Next Generation One of the most rewarding parts of this role? You'll coach and guide junior Data Management Leads, helping them grow while raising the overall capability of the team. Your expertise becomes their foundation. Representing DM at the Highest Level You'll sit at the table for cross-functional project teams and regulatory submission teams, and you'll be a key player during Health Authority inspections and audits. This is a role where your voice carries real weight. Vendor Oversight & Partnerships Whether working with FSPs, CROs, or third-party vendors, you'll be the quality compass; monitoring deliverables, managing data currency throughout the trial, and holding partners accountable to SLAs that protect the integrity of our work. Driving Continuous Improvement You'll contribute meaningfully to how we evolve as an organisation - supporting CAPA implementation and bringing fresh thinking to continuous improvement initiatives within Clinical Data Management. What's In It For You Meaningful impact , your work directly supports the development of medicines that matter to millions of patients globally Career elevation , step into a senior leadership role with visibility across R&D and a clear path toward Director-level progression Cross-functional influence, build relationships across clinical operations, regulatory, biostatistics, and beyond Industry exposure , travel to conferences, investigator meetings, and regulatory engagements (approximately 5-10% travel) to stay at the forefront of your field Intellectual challenge , work with cutting-edge data collection technologies and emerging industry trends that keep your skills sharp and future-proof What You'll Bring A Bachelor's Degree (advanced degree preferred) and at least 5 years of relevant industry experience A strong command of clinical drug development processes, FDA/ICH guidelines, and data management best practices Hands-on experience with EDC systems; Medidata RAVE experience is a strong plus Proven project management skills, with a PMP certification considered a bonus The ability to translate complex data into clear insights through metrics analysis and reporting Outstanding communication skills, whether you're presenting to senior leadership or collaborating with a vendor team, you know how to land the message Familiarity with submission requirements including NDA, BLA, and MAA processes Ready to Apply? If you're someone who takes pride in doing rigorous work and inspiring others to do the same, someone who sees clinical data not just as numbers, but as the foundation of scientific truth, we'd love to hear from you. Join BMS. Transform patients' lives. Build your own. If you come across a role that intrigues you but doesn't perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career. Uniquely Interesting Work, Life-changing Careers With a single vision as inspiring as "Transforming patients' lives through scienceTM ", every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues. On-site Protocol BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function. Supporting People with Disabilities BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to . Visit to access our complete Equal Employment Opportunity statement.Bristol Myers Squibb is Disability Confident - EmployerA UK Government scheme Candidate Rights BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area. Data Protection We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at . Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley.R : Senior Manager, Clinical Data Management
02/07/2026
Full time
Senior Manager, Clinical Data ManagementUxbridge - GBFind out how well you match with this job Working with Us Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: Are you ready to do the work of your career? At Bristol Myers Squibb, we believe that the right data, in the right hands, at the right time can change everything. Every clinical trial we run brings us closer to a treatment that could transform or save a patient's life.As our Senior Manager of Clinical Data Management, you'll be the person who makes that possible. This isn't just a data role. It's a leadership position at the heart of our R&D pipeline; where your decisions, your standards, and your expertise directly shape the speed and quality of life-changing medicines reaching patients worldwide. What You'll Be Doing Leading Where It Matters Most You'll take the wheel on end-to-end clinical data management for some of our most complex and impactful trials. That means being the go-to person for both internal teams and external partners, the one who sets the bar for data quality and makes sure everyone clears it. Drive data collection strategy across one or more complex clinical development projects, aligning cross-functional teams around clear, high-quality standards Own the full data management lifecycle, from planning and collection through to clean, submission-ready datasets delivered on time Shape the systems that power our trials, leading requirements gathering for EDC platforms and collaborating with partners across eCOA, External Data, and Safety Gateway Chair Data Quality Review meetings to keep trial data current, complete, and audit-ready at every stage Author and review key study documents, Data Quality Management Plans, Data Validation Plans, eCRF Completion Guidelines and more, ensuring consistency and compliance across the board Mentoring the Next Generation One of the most rewarding parts of this role? You'll coach and guide junior Data Management Leads, helping them grow while raising the overall capability of the team. Your expertise becomes their foundation. Representing DM at the Highest Level You'll sit at the table for cross-functional project teams and regulatory submission teams, and you'll be a key player during Health Authority inspections and audits. This is a role where your voice carries real weight. Vendor Oversight & Partnerships Whether working with FSPs, CROs, or third-party vendors, you'll be the quality compass; monitoring deliverables, managing data currency throughout the trial, and holding partners accountable to SLAs that protect the integrity of our work. Driving Continuous Improvement You'll contribute meaningfully to how we evolve as an organisation - supporting CAPA implementation and bringing fresh thinking to continuous improvement initiatives within Clinical Data Management. What's In It For You Meaningful impact , your work directly supports the development of medicines that matter to millions of patients globally Career elevation , step into a senior leadership role with visibility across R&D and a clear path toward Director-level progression Cross-functional influence, build relationships across clinical operations, regulatory, biostatistics, and beyond Industry exposure , travel to conferences, investigator meetings, and regulatory engagements (approximately 5-10% travel) to stay at the forefront of your field Intellectual challenge , work with cutting-edge data collection technologies and emerging industry trends that keep your skills sharp and future-proof What You'll Bring A Bachelor's Degree (advanced degree preferred) and at least 5 years of relevant industry experience A strong command of clinical drug development processes, FDA/ICH guidelines, and data management best practices Hands-on experience with EDC systems; Medidata RAVE experience is a strong plus Proven project management skills, with a PMP certification considered a bonus The ability to translate complex data into clear insights through metrics analysis and reporting Outstanding communication skills, whether you're presenting to senior leadership or collaborating with a vendor team, you know how to land the message Familiarity with submission requirements including NDA, BLA, and MAA processes Ready to Apply? If you're someone who takes pride in doing rigorous work and inspiring others to do the same, someone who sees clinical data not just as numbers, but as the foundation of scientific truth, we'd love to hear from you. Join BMS. Transform patients' lives. Build your own. If you come across a role that intrigues you but doesn't perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career. Uniquely Interesting Work, Life-changing Careers With a single vision as inspiring as "Transforming patients' lives through scienceTM ", every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues. On-site Protocol BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function. Supporting People with Disabilities BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to . Visit to access our complete Equal Employment Opportunity statement.Bristol Myers Squibb is Disability Confident - EmployerA UK Government scheme Candidate Rights BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area. Data Protection We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at . Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley.R : Senior Manager, Clinical Data Management
Bristol-Myers Squibb in Uxbridge is searching for a Senior Manager of Clinical Data Management. In this leadership role, you will oversee data management for critical clinical trials, ensuring high standards of data quality and compliance. You will drive data collection strategies, mentor junior staff, and collaborate with cross-functional teams to ensure timely and accurate data delivery. This position offers significant career advancement opportunities and the chance to make a real impact on patient lives.
01/07/2026
Full time
Bristol-Myers Squibb in Uxbridge is searching for a Senior Manager of Clinical Data Management. In this leadership role, you will oversee data management for critical clinical trials, ensuring high standards of data quality and compliance. You will drive data collection strategies, mentor junior staff, and collaborate with cross-functional teams to ensure timely and accurate data delivery. This position offers significant career advancement opportunities and the chance to make a real impact on patient lives.