Associate Director, Medical Scientist, US Medical Oncology, Relatlimab/Melanoma
3 weeks ago
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.
Position Summary
Position reports to the Director of US Medical Oncology, Melanoma/Relatlimab. The primary responsibility of the Associate Director is developing and implementing the US Medical strategies, objectives and launch priorities in Melanoma with a strong focus on Relatlimab. This Associate Director role is responsible for leading the integration and alignment of relatlimab strategies through establishing and maintaining cross-functional collaborative relationships with key stakeholders including, but not limited to, US Commercialization, WW Medical, Clinical Development, Medical Capabilities teams, etc.
Key Responsibilities
Lead the development of the US medical plan for melanoma and relatlimab in alignment with US Commercial and WW Medical
Provide strategic, scientific, and executional leadership while partnering with the integrated matrix team, including Medical, Commercial and Access organizations
Lead and partner effectively with the integrated matrix team for medical-related activities and tactics
Develop/refine and implement key medical activities, including medical advisory boards, Scientific Engagement Partner resources and training, congresses, reactive content, and communication strategy, including publications
Establish US Medical data generation strategies and collaborate with Medical Evidence Generation to oversee the execution of the Investigator Sponsored Research programs from concept through full execution, including reporting the evidence at scientific congresses, in peer reviewed publications, and proactive/reactive BMS communication tools.
Collaborate within US Medical matrix teams (Field Medical, Data Generation, Patient Advocacy, Medical Education, and Congress Management) to plan and deliver medical objectives with flawless execution and excellent budget utilization.
Partner with US Commercial and Access organizations to integrate medical perspectives into the commercial strategy and ensure appropriate alignment between commercial and medical activities
Develop and maintain long-term, trusted relationships with external thought Leaders and scientific experts to assess unmet medical needs to develop appropriate medical strategies.
Collaborates with functional areas outside of medical including marketing, sales, access, legal, regulatory, clinical operations, and research and development
Ensure US medical strategies, objectives and tactics are aligned across the medical matrix and integrated with the strategic brand plan
Qualifications & Experience
Advanced scientific degree (MD, PhD, PharmD, DNP)
Prior (3-5+ years) pharmaceutical industry experience in medical affairs is required
Highly organized and motivated individual with the ability to lead multiple projects and initiatives across diverse high performing matrix teams
Possess excellent communication and presentation skills, both verbal and written
He or she should understand pharmaceutical drug development, including clinical development, regulatory, life cycle management of pharmaceutical products, and knowledge of Thought Leaders in the field
Must have strong interpersonal and communication skills to navigate complex situations and gain alignment with diverse stakeholders, and work effectively within cross-functional teams
Demonstrated ability to execute and deliver results in a deadline-driven environment while managing multiple priorities
Estimated 20% travel (as applicable)
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