Senior Director, Immunology, Cardiovascular, & Neuroscience, Medical Evidence Generation
Bristol Myers Squibb
2 months ago
On-site
Madison, NJ
Medical Affairs
Responsibilities:
- Build, manage, and coach an externally focused global team accountable for defining and executing the I,CV,&N portfolio to address key data gaps.
- Coach MEG Leads (including Clinical Scientists and Clinical Trial Physicians) to oversee Medical clinical trials end-to-end (start-up; influence governance outcomes; partner on agreement initiation/negotiation/execution; oversee throughout study and support readout).
- Design and drive strategies to identify and advance new medical trials that accelerate the BMS pipeline.
- Provide project leadership for cross-functional teams focused on scientific aspects (including results) and study-related activities.
- Contribute to the evolution of the MEG organizational model and operational infrastructure.
- Ensure the I,CV,&N MEG book of work (MASTs, ISRs, CRCs, and IEP development) aligns with the Integrated Evidence Plan (IEP) and is executed with rigor and on time.
- Oversee authoring/development of medical study protocol and ICF; provide medical input to ensure clinical relevance, scientific rigor, patient safety, and alignment with study objectives.
- Ensure scientific integrity and data quality throughout medical trial execution (start-up/conduct/closure).
- Lead co-development and maintenance of IEPs with Medical, HEOR, Development, and other stakeholders.
- Partner with stakeholders across Medical Affairs and Drug Development to ensure cohesiveness and “one MEG voice.”
- Use business acumen and fiscal stewardship to create reciprocal scientific value and allocate resources consistent with company priorities.
- Assist in concept reviews through the RFP process (context for ongoing work, area-of-interest development, and upcoming data readouts).
Qualifications & Experience:
- MD preferred (or x-US equivalent).
- 5+ years required clinical trial experience in a pharmaceutical industry setting (e.g., Clinical Trial Physician, Clinical Scientist); expertise in drug development process and clinical research; demonstrated ability to drive/manage company-sponsored clinical trials and lead teams.
- 5+ years preferred strategic leadership experience in pharma; in-depth understanding of clinical and business development, Medical Affairs, and Commercial functions related to drug development.
- 10+ years preferred in clinical science, clinical research, or equivalent.
- Professional diplomacy; communicates effectively and influences decision-making at all levels.
- Promotes scientific excellence, multidisciplinary problem solving, teamwork, execution, quality, and communication.
- Builds credibility with external investigators and collaborators; balances business and scientific acumen; enterprise mindset.
- Demonstrated ability to build and sustain high-performing teams and lead in complex, matrix environments.
Location/Travel:
- Preferably based at Princeton Pike (PPK) site in Lawrenceville, NJ; expected travel ~20%-30% globally.
Benefits (as stated):
- Health coverage (medical, pharmacy, dental, vision); wellbeing support; financial wellbeing/protection (401(k), disability, life insurance, accident insurance, supplemental health, business travel protection, personal liability protection, identity theft benefit, legal support, survivor support); Paid Time Off (flexible time off for US Exempt employees; annual paid vacation and holidays for certain other employee groups); additional time off as eligibility-based.
- Global Shutdown between Christmas and New Year’s Day (eligibility-based).
Compensation (as stated):
- $229,380–$277,956 (Madison-Giralda, NJ and Princeton, NJ).
Application instruction (as stated):
- If you’re interested but not a perfect resume match, BMS encourages you to apply anyway.
- Build, manage, and coach an externally focused global team accountable for defining and executing the I,CV,&N portfolio to address key data gaps.
- Coach MEG Leads (including Clinical Scientists and Clinical Trial Physicians) to oversee Medical clinical trials end-to-end (start-up; influence governance outcomes; partner on agreement initiation/negotiation/execution; oversee throughout study and support readout).
- Design and drive strategies to identify and advance new medical trials that accelerate the BMS pipeline.
- Provide project leadership for cross-functional teams focused on scientific aspects (including results) and study-related activities.
- Contribute to the evolution of the MEG organizational model and operational infrastructure.
- Ensure the I,CV,&N MEG book of work (MASTs, ISRs, CRCs, and IEP development) aligns with the Integrated Evidence Plan (IEP) and is executed with rigor and on time.
- Oversee authoring/development of medical study protocol and ICF; provide medical input to ensure clinical relevance, scientific rigor, patient safety, and alignment with study objectives.
- Ensure scientific integrity and data quality throughout medical trial execution (start-up/conduct/closure).
- Lead co-development and maintenance of IEPs with Medical, HEOR, Development, and other stakeholders.
- Partner with stakeholders across Medical Affairs and Drug Development to ensure cohesiveness and “one MEG voice.”
- Use business acumen and fiscal stewardship to create reciprocal scientific value and allocate resources consistent with company priorities.
- Assist in concept reviews through the RFP process (context for ongoing work, area-of-interest development, and upcoming data readouts).
Qualifications & Experience:
- MD preferred (or x-US equivalent).
- 5+ years required clinical trial experience in a pharmaceutical industry setting (e.g., Clinical Trial Physician, Clinical Scientist); expertise in drug development process and clinical research; demonstrated ability to drive/manage company-sponsored clinical trials and lead teams.
- 5+ years preferred strategic leadership experience in pharma; in-depth understanding of clinical and business development, Medical Affairs, and Commercial functions related to drug development.
- 10+ years preferred in clinical science, clinical research, or equivalent.
- Professional diplomacy; communicates effectively and influences decision-making at all levels.
- Promotes scientific excellence, multidisciplinary problem solving, teamwork, execution, quality, and communication.
- Builds credibility with external investigators and collaborators; balances business and scientific acumen; enterprise mindset.
- Demonstrated ability to build and sustain high-performing teams and lead in complex, matrix environments.
Location/Travel:
- Preferably based at Princeton Pike (PPK) site in Lawrenceville, NJ; expected travel ~20%-30% globally.
Benefits (as stated):
- Health coverage (medical, pharmacy, dental, vision); wellbeing support; financial wellbeing/protection (401(k), disability, life insurance, accident insurance, supplemental health, business travel protection, personal liability protection, identity theft benefit, legal support, survivor support); Paid Time Off (flexible time off for US Exempt employees; annual paid vacation and holidays for certain other employee groups); additional time off as eligibility-based.
- Global Shutdown between Christmas and New Year’s Day (eligibility-based).
Compensation (as stated):
- $229,380–$277,956 (Madison-Giralda, NJ and Princeton, NJ).
Application instruction (as stated):
- If you’re interested but not a perfect resume match, BMS encourages you to apply anyway.