Director – Medical – Pulmonary
| Company | Bristol Myers Squibb |
|---|---|
| Location | Lawrence Township, NJ, USA |
| Salary | $Not Provided – $Not Provided |
| Type | Full-Time |
| Degrees | PharmD, PhD, MD |
| Experience Level | Senior, Expert or higher |
Requirements
- Advanced scientific degree (MD, PhD, PharmD, PA/NP)
- Prior (5-10+ years) pharmaceutical industry experience in medical affairs is preferred
- Highly organized and motivated individual with the ability to lead multiple projects and initiatives across diverse high performing matrix teams
- Ability to work effectively within cross-functional teams
- Excellent communication and presentation skills, both verbal and written
- Understanding of pharmaceutical drug development including clinical development, regulatory, life cycle management of pharmaceutical products
- Knowledge of thought leaders in the field
- Clinical expertise and relevant experience in the disease area within the pharmaceutical industry, such as within Medical Affairs or Clinical Development
- Ability to lead and develop people
- Strong interpersonal and communication skills to navigate complex situations and gain alignment with diverse stakeholders
- Demonstrated ability to execute and deliver results in a deadline-driven environment while managing multiple priorities
- Strong understanding of business acumen including payer and market access challenges
- Travel: Expected 20% travel within the continental US
Responsibilities
- Provide input and advice to conduct the review of promotional materials for scientific/medical validity
- Participate in internal and external meetings to remain current on changing regulations, relevant new medical/scientific information and commercial strategy
- Establish clear and challenging goals that allow skilled and empowered professionals to accomplish business objectives
- Support the execution of US medical plan that is both product and disease specific in alignment with US Commercialization (USC) and WW Medical (WWM)
- Establish US Medical data generation strategies and collaborate with Medical Data Generation (MDG) to oversee the execution of the Investigator Sponsored Research (ISR) programs
- Partner closely with colleagues in Discovery, Clinical Research, Regulatory, and Health Outcomes to ensure the science of the pipeline products and marketed medicines are understood and communicated properly
- Engage with high impact external thought leaders to identify and translate key insights and to drive adoption of BMS medicines
- Contribute to shape the competitive strategies around pricing and reimbursement
- Demonstrate the ability to make effective decisions on selecting external organizations and researchers for research collaborations
- Participate in mentoring, coaching and training of new and existing colleagues
Preferred Qualifications
- Prior (5-10+ years) pharmaceutical industry experience in medical affairs is preferred
- The ideal candidate will have clinical expertise and some relevant experience in the disease area within the pharmaceutical industry, such as within Medical Affairs or Clinical Development