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 rich in diversity. 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: careers.bms.com/working-with-us.
Functional Area Description
- The Worldwide Patient Safety (WWPS) group is responsible for ensuring the safety of our medicines. WWPS pharmacovigilance and pharmacoepidemiology deliverables include single case and aggregate safety monitoring, safety reporting, contributing to benefit-risk assessment, risk management planning and strategy, execution of certain post marketing commitments, and ensuring compliance with global regulatory requirements.
Position Summary
- Lead safety activities and benefit-risk strategies for assigned BMS compounds/programs in the Immunology Therapeutic Area (TA) and chair the product Safety Management Team(s).
- Oversee, prepare, and/or review aggregate safety review documents as well as safety sections of relevant clinical trial documents and regulatory filings.
- Lead team in the evaluation & management of signals emerging from any data source. Develop strategy for signal evaluation and document outcome.
- Lead safety labeling activities for assigned products/program. Act as the Safety Subject Matter Expert for input to regulatory product labeling. Participate/provide input at cross-functional labeling team meetings and provide regional safety labeling support.
- Lead process improvement projects. Assist the Medical Safety Assessment (MSA) TA Head/Lead in developing and maintaining state-of-the-art Pharmacovigilance (PV) processes and procedures within BMS Drug Development and WWPS.
- Support the EU Qualified Person for PV or other regional or local Qualified Person for PV relative to issues relating to assigned products.
- Provide input to Drug Development publication strategy/plan & ensure safety input to publications/presentations.
- Actively drive safety strategy preparation and represent WWPS at Health Authority (HA) and Data Monitoring Committee (DMC) meetings.
- Ensure that the above tasks are performed in the most efficient manner possible commensurate with quality, accuracy, and timeliness and in accordance with current global regulatory requirements and BMS cost effectiveness goals.
- Promote collegiality and teamwork among peers. Mentor/support colleagues as a positive change agent.
Position Responsibilities
General Product Support
- Lead safety activities and benefit-risk strategies for assigned BMS compounds and chair the product SMT(s).
- Oversee, prepare, and/or review aggregate safety review documents (e.g., Development Safety Update Reports [DSUR], Periodic Benefit-Risk Evaluation Reports [PBRER]) and safety sections of relevant clinical trial documents (e.g., protocols, clinical study reports [CSR], investigator brochures [IB], informed consent forms [ICF]) and regulatory filings (e.g., clinical trial applications, marketing authorization applications).
- Lead team in evaluation & management of signals emerging from any data source. Develop strategy for signal evaluation (egg, case-series, literature review, HA/ claims database). Document by Safety Topic Review/ Signal Report or other means of communication.
- Lead safety labeling activities for assigned products. Act as the Safety Subject Matter Expert for input to regulatory product labeling. Participate/provide input at cross-functional labeling team meetings and provide regional safety labeling support.
- Support the EU QPPV or other regional or local Qualified Person for PV relative to issues relating to assigned products.
- Provide input to Drug Development publication strategy/plan & ensure safety input to publications/presentations.
Clinical Development
- Act as the global safety lead for assigned compounds in development. Provide safety lead support for global submission document production. Review draft summary documents.
- Lead medical safety development and execution of benefit-risk management strategies for assigned products.
- Provide safety input to clinical development plans, study protocols, amendments, IB, statistical analysis plan, ICF, CSR, responses to HA or institutional review board/ ethics committee queries.
- Lead development of safety risk language, risk management strategy, pre-filing safety activities including safety table shells, integrated safety data review, integrated safety summary document review, and safety-focused publication development.
- Perform medical safety review of DSUR, annual reports and other periodic safety submissions.
- Support safety strategy preparation for pre-submission meetings, Advisory Committee meetings, Scientific Advice meetings, DMC meetings, etc.
- Post marketing Support
- Act as the safety lead for assigned marketed compounds and support global post marketing safety activities and submissions.
- Provide medical safety, benefit-risk input for safety aggregate reports, product renewal submissions, post marketing study documents and reports, responses to HA queries.
- Lead medical safety oversight of and execution of risk management strategies and RMP elements for assigned products.
- Lead safety signal evaluation & management. Prepare and review reports on safety signals (ie, Safety Topic Reviews/Signal Reports) and ad hoc regulatory responses.
- Provide post marketing safety study guidance to other groups including epidemiology and medical affairs including but not limited to investigator-sponsored research, epidemiology studies, and non-interventional safety studies.
- Ensure safety labeling adequately reflects emerging post marketing safety profile.
Department Activities
- Lead process improvement projects. Assist the MSA TA Head/Lead in developing and maintaining state-of-the-art PV processes and procedures within BMS Drug Development and WWPS.
- Support preparation for regulatory inspections with evaluation of current processes and assess alignment with regulatory expectations, guidelines, and mandates.
- Assist the team and senior management in all forms of issue management and crisis management.
- Liaise with all TA staff and maintain an effective and collaborative patient safety team.
- Support hiring & orientation.
Cross-Functional Activities
- Provide input to strategic plans for safety differentiation of BMS products.
- Prepare and provide training to BMS employees on product safety profiles/issues.
- Act as WWPS liaison for assigned products with BMS functions (Legal, Business Development, Operations, Marketing, etc.).
- Support manufacturing quality. Co-Author integrated health hazard assessments.
- Develop communications of safety data & interpretation to BMS and external parties, globally.
Degree Requirements
- MD/equivalent required. Postgraduate qualification or experience in internal medicine, immunology, or related specialty desirable.
- Experience Requirements
- 3+ years in PV or relevant pharmaceutical or biomedical field (eg, Medical, Clinical, Regulatory) is strongly preferred. Other relevant experiences & accomplishments considered, such as roles in clinical research, observational research & clinical practice experience.
Key Competency Requirements
Position Summary
- Lead safety activities and benefit-risk strategies for assigned BMS compounds/programs in the Immunology Therapeutic Area (TA) and chair the product Safety Management Team(s).
- Oversee, prepare, and/or review aggregate safety review documents as well as safety sections of relevant clinical trial documents and regulatory filings.
- Lead team in the evaluation & management of signals emerging from any data source. Develop strategy for signal evaluation and document outcome.
- Lead safety labeling activities for assigned products/program. Act as the Safety Subject Matter Expert for input to regulatory product labeling. Participate/provide input at cross-functional labeling team meetings and provide regional safety labeling support.
- Lead process improvement projects. Assist the Medical Safety Assessment (MSA) TA Head/Lead in developing and maintaining state-of-the-art Pharmacovigilance (PV) processes and procedures within BMS Drug Development and WWPS.
- Support the EU Qualified Person for PV or other regional or local Qualified Person for PV relative to issues relating to assigned products.
- Provide input to Drug Development publication strategy/plan & ensure safety input to publications/presentations.
- Actively drive safety strategy preparation and represent WWPS at Health Authority (HA) and Data Monitoring Committee (DMC) meetings.
- Ensure that the above tasks are performed in the most efficient manner possible commensurate with quality, accuracy, and timeliness and in accordance with current global regulatory requirements and BMS cost effectiveness goals.
- Promote collegiality and teamwork among peers. Mentor/support colleagues as a positive change agent.
Position Responsibilities
General Product Support
- Lead safety activities and benefit-risk strategies for assigned BMS compounds and chair the product SMT(s).
- Oversee, prepare, and/or review aggregate safety review documents (e.g., Development Safety Update Reports [DSUR], Periodic Benefit-Risk Evaluation Reports [PBRER]) and safety sections of relevant clinical trial documents (e.g., protocols, clinical study reports [CSR], investigator brochures [IB], informed consent forms [ICF]) and regulatory filings (e.g., clinical trial applications, marketing authorization applications).
- Lead team in evaluation & management of signals emerging from any data source. Develop strategy for signal evaluation (egg, case-series, literature review, HA/ claims database). Document by Safety Topic Review/ Signal Report or other means of communication.
- Lead safety labeling activities for assigned products. Act as the Safety Subject Matter Expert for input to regulatory product labeling. Participate/provide input at cross-functional labeling team meetings and provide regional safety labeling support.
- Support the EU QPPV or other regional or local Qualified Person for PV relative to issues relating to assigned products.
- Provide input to Drug Development publication strategy/plan & ensure safety input to publications/presentations.
Clinical Development
- Act as the global safety lead for assigned compounds in development. Provide safety lead support for global submission document production. Review draft summary documents.
- Lead medical safety development and execution of benefit-risk management strategies for assigned products.
- Provide safety input to clinical development plans, study protocols, amendments, IB, statistical analysis plan, ICF, CSR, responses to HA or institutional review board/ ethics committee queries.
- Lead development of safety risk language, risk management strategy, pre-filing safety activities including safety table shells, integrated safety data review, integrated safety summary document review, and safety-focused publication development.
- Perform medical safety review of DSUR, annual reports and other periodic safety submissions.
- Support safety strategy preparation for pre-submission meetings, Advisory Committee meetings, Scientific Advice meetings, DMC meetings, etc.
- Post marketing Support
- Act as the safety lead for assigned marketed compounds and support global post marketing safety activities and submissions.
- Provide medical safety, benefit-risk input for safety aggregate reports, product renewal submissions, post marketing study documents and reports, responses to HA queries.
- Lead medical safety oversight of and execution of risk management strategies and RMP elements for assigned products.
- Lead safety signal evaluation & management. Prepare and review reports on safety signals (ie, Safety Topic Reviews/Signal Reports) and ad hoc regulatory responses.
- Provide post marketing safety study guidance to other groups including epidemiology and medical affairs including but not limited to investigator-sponsored research, epidemiology studies, and non-interventional safety studies.
- Ensure safety labeling adequately reflects emerging post marketing safety profile.
Department Activities
- Lead process improvement projects. Assist the MSA TA Head/Lead in developing and maintaining state-of-the-art PV processes and procedures within BMS Drug Development and WWPS.
- Support preparation for regulatory inspections with evaluation of current processes and assess alignment with regulatory expectations, guidelines, and mandates.
- Assist the team and senior management in all forms of issue management and crisis management.
- Liaise with all TA staff and maintain an effective and collaborative patient safety team.
- Support hiring & orientation.
Cross-Functional Activities
- Provide input to strategic plans for safety differentiation of BMS products.
- Prepare and provide training to BMS employees on product safety profiles/issues.
- Act as WWPS liaison for assigned products with BMS functions (Legal, Business Development, Operations, Marketing, etc.).
- Support manufacturing quality. Co-Author integrated health hazard assessments.
- Develop communications of safety data & interpretation to BMS and external parties, globally.
Degree Requirements
- MD/equivalent required. Postgraduate qualification or experience in internal medicine, immunology, or related specialty desirable.
- Experience Requirements
- 3+ years in PV or relevant pharmaceutical or biomedical field (eg, Medical, Clinical, Regulatory) is strongly preferred. Other relevant experiences & accomplishments considered, such as roles in clinical research, observational research & clinical practice experience.
Key Competency Requirements
- Understanding of the drug development process.
- Knowledge of PV and ability to apply knowledge to evaluation of safety concerns and minimization of patient risk throughout the life cycle of a drug product.
- Proficient ability to leverage the range of available tools to investigate safety concerns, including the science of observational research.
- Understanding of regulatory requirements for safety assessment and action.
- Strong scientific analytical reasoning skills.
- Ability to work on multiple projects in parallel.
- Excellent attention to detail.
- Behavioral competencies necessary to work and lead within a complex matrix environment.
- Excellent verbal and written communication skills.
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 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 an inclusive culture, promoting diversity 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 a diverse 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.
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 adastaffingsupport@bms.com. Visit careers.
