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Associate Director, US Medical Promotional Review Scientist, Immunology/Cardiovascular

Bristol Myers Squibb
Full-time
Remote friendly (Princeton, NJ)
United States
Medical Affairs

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Role Summary

Associate Director, US Medical Promotional Review Scientist, Immunology/Cardiovascular — The Associate Director serves as a strategic, solutions-oriented partner focused on ensuring the medical accuracy and scientific validity of promotional and non-promotional materials within Global Medical Affairs.

Responsibilities

  • Maintain therapeutic area and product knowledge through ongoing assessment of relevant published literature, treatment guidelines, internal resources, and data.
  • Provide strong medical guidance in interdisciplinary meetings and related initiatives, including promotional review, disease/brand and launch planning, labeling changes, and business reviews.
  • As a member of the Medical Promotional Review (PReP) team, conduct reviews of promotional and proactive materials for scientific and medical validity.
  • Critically evaluate and offer strategically sound solutions for complex promotional and non-promotional tactics to ensure message balance, key clinical findings, medical accuracy, and content appropriateness in accordance with relevant guidelines.
  • Proactively align and build strong relationships with marketing, access, medical, corporate communications, training, legal, and commercial regulatory affairs to ensure balanced messaging.
  • Demonstrate leadership within the medical review team to drive best practices aligned with strategic imperatives; participate in process-improvement initiatives.
  • Provide medical advice and guidance on draft product labeling to ensure commercially viable US labeling for future promotion and advertising.
  • Participate in internal and external meetings to stay current on regulations, medical/scientific developments, and commercial strategy.
  • Assess the acceptability of data/references used to support promotional claims and provide expert guidance to resolve issues and approve materials.
  • Stay informed of industry trends and promote best practice sharing across medical and promotional review teams.
  • Complete all assigned SOPs and training within designated timeframes and adhere to job-specific SOPs and work instructions.
  • Conduct business in accordance with BMS Values.

Qualifications

  • Advanced scientific degree (PharmD, PhD, or MD preferred).
  • Minimum of 3-5 years of clinical practice or pharmaceutical/healthcare industry experience; therapeutic area experience preferred.
  • Thorough understanding of medical writing and promotional material review in the pharmaceutical industry.
  • Proven ability to manage multiple projects, solve problems, deliver on commitments, and work with multidisciplinary teams.
  • Strong scientific/medical written and verbal communication skills.
  • Knowledge of the pharmaceutical industry and external compliance, transparency, and conflict-of-interest environments.
  • Experience delivering customer-focused service.
  • Flexibility in response to changing needs and competing demands.
  • Developed business acumen and ability to influence senior internal stakeholders.
  • Strong team player with individual initiative and accountability.
  • Strong leadership and organizational skills with demonstrated success in driving optimal business results in a complex matrix organization.
  • Strategic leadership, performance management, alignment building, negotiation, and collaboration skills.
  • Proven ability to work in an ambiguous environment.
  • Experience working on teams through change and navigating complex organizational dynamics.
  • Ability to analyze and interpret trial data; experience with FDAMA 114 content, Real World Evidence, and other data consistent with FDA-approved labeling (CFL).
  • Strong stakeholder relationship-building and negotiation skills.
  • Ability to travel 10-25% (domestically and internationally).

Skills

  • Medical writing and promotional material review
  • Strategic collaboration and cross-functional partnership
  • Regulatory and compliance knowledge (FDA/OPDP)
  • Data interpretation and evidence-based decision making

Education

  • Advanced scientific degree (PharmD, PhD, or MD preferred).
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