Bristol Myers Squibb

Director, Lead Cardiovascular, Medical Evidence Generation

Bristol Myers Squibb

full-time

Posted on:

Location Type: Office

Location: Princeton • New Jersey • 🇺🇸 United States

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Salary

💰 $207,490 - $251,433 per year

Job Level

Senior

About the role

  • Responsible for implementation, planning, and scientific execution of CV MEG Book of Work (BoW) in different study modalities, CRCs, ISRs and MASTs.
  • Work closely with other study team members within the assigned project to execute activities associated with the conduct.
  • Successfully leads, plans, and executes end-to-end trial level activities, including study startup, conduct and close-out activities as applicable.
  • Facilitate collaborative exchange between BMS, Investigators and thought leaders in community practice and academia, including scientific dialogue and representing BMS as a trusted, inclusive, and innovative industry collaborator and partner of choice.
  • Develop key study documents as concept, protocol, ICF and CRF; including writing, reviewing, adjudication/resolution of cross functional comments and ensuring high clinical quality (collaboration with the assigned Medical Writer if applicable).
  • Ensure CRF design adequately supports data collection in alignment with the protocol (in collaboration with Data Management and Programming teams).
  • Preparation of study documents for governance review and approval.
  • Provide training and serve as point of contact for clinical questions at study sites.
  • Lead database lock/snapshot readiness (in collaboration with Data Management and Biostats teams), data review, and cleaning, and prepare for topline results readout.
  • Act as point of contact for CRCs, ISRs, and MASTs within Therapeutic and Disease area teams.
  • Proactively design and drive strategies to accelerate the CV MEG BoW leveraging external research platforms, technologies, and insights.
  • Align with and advise senior functional and therapeutic area leaders on new external opportunities that will inform strategy and influence decisions in the creation/refinement of integrated evidence generation plans.
  • Lead a limited number of high-visibility projects leveraging relevant disease subject matter expertise.
  • Contribute to the evolution of MEG therapeutic area strategy and value proposition.

Requirements

  • Advanced scientific degree (MD, PhD, PharmD, MS or the equivalent) required with extensive, relevant scientific, and/or clinical experience.
  • At least 5 years of experience in pharmaceutical clinical development, Medical Affairs, or relevant Commercial experience; previous customer-facing role experience highly desirable.
  • Required previous experience in writing study protocols, database lock/snapshots readiness (including data review and data cleaning) and preparation for topline results readout.
  • Preferred previous experience in observational studies.
  • Preferred previous experience in Cardiovascular.
Benefits
  • Medical, pharmacy, dental and vision care.
  • Wellbeing support such as the BMS Living Life Better program and employee assistance programs (EAP).
  • Financial well-being resources and a 401(K).
  • Financial protection benefits such as short- and long-term disability, life insurance, supplemental health insurance, business travel protection and survivor support.
  • Work-life programs include paid national holidays and optional holidays, Global Shutdown Days between Christmas and New Year’s holiday, up to 120 hours of paid vacation, up to two (2) paid days to volunteer, sick time off, and summer hours flexibility.
  • Parental, caregiver, bereavement, and military leave.
  • Family care services such as adoption and surrogacy reimbursement, fertility/infertility benefits, support for traveling mothers, and child, elder and pet care resources.
  • Other perks like tuition reimbursement and a recognition program.

Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard skills
clinical trial managementstudy protocol writingdata reviewdata cleaningdatabase lock readinesstopline results preparationobservational studiesscientific executionclinical quality assurancecross-functional collaboration
Soft skills
leadershipcollaborationcommunicationstrategic planningproblem-solvingtrainingrelationship managementinclusivityinnovationscientific dialogue
Certifications
MDPhDPharmDMS