Medical Director US Medical Affairs Multiple Myeloma

Profile

Bristol-Myers Squibb is a global Biopharma company committed to a single mission: to discover, develop, and deliver innovative medicines focused on helping millions of patients around the world in disease areas such as oncology, cardiovascular, immunoscience and fibrosis.

Join us and make a difference. We hire the best people and provide them with a work environment that places a premium on diversity, integrity, collaboration and personal development. Through a culture of inclusion, we create a better, more productive work environment. We believe that the diverse experiences and perspectives of all our employees help to drive innovation and transformative business results.

Summary/Scope:

The Medical Director, US Medical Affairs will report to the Disease Lead, USMA. He/she will be headquarters based in Summit, New Jersey and will provide scientific/medical leadership and support for compounds in various stages of clinical development, as well as approved products in that therapeutic area. This individual will support the design and implementation of an integrated medical plan within the US, under the direction of Disease Lead, USMA, and in coordination with the Global cross-functional teams. Together, they will take an ownership role in leading the execution of Celgene/BMS-sponsored medical affairs trials and will also be responsible for the evaluation and support of investigator-initiated trials. He/she will represent US Medical Affairs as needed, serving as a therapeutic area expert in strategic and tactical discussions and presentations with internal colleagues, including the US and Global cross-functional teams, as well as external experts and investigators.

Responsibilities will include, but are not limited to, the following:

Strategic and Tactical Planning: Responsibility for the Medical Affairs aspects of the following plans, in alignment with global plans, and their timely updates:

Brand plans

Launch plans for new products or new indication launches

Publication plans

Strategic and tactical plan

Responsible for the planning and timely execution of Medical Affairs Sponsored Trials, within appropriate standards for compliance, quality, timeliness, and budget. Lead various activities of US and Global cross-functional teams relating to medical affairs. Represent US Medical Affairs as a therapeutic area expert in both internal and external venues including the US and Global cross-functional teams, clinical sub-teams, and advisory boards / steering committees. Lead/support various Medical Affairs cross-functional working groups. Represent Celgene at professional meetings, congresses, and local symposia. Collaborate with Medical Affairs colleagues to define, guide and execute therapeutic regional strategies and tactics with appropriate use of resources. Provide high quality clinical input and review of: Disease strategy plans, abstracts, posters, slides, manuscripts, educational materials, IIT protocols, steering committee and advisory board meeting objectives, Medical information letters, Commercial Brand plans, Scientific educational grant requests and patient advocacy grant requests Track priority Medical Affairs tactics and performance to goals/budget Perform research and analytics and provide recommendations to support quality medical decisions regarding clinical research, consultancy, and internal planning. Partner with Scientific Communications on developing timely publication strategy and plan, gap analysis, and key messages. Assist with data summaries, preparation for site visits/corporate visits/payor presentations. Interaction with key stakeholders, as a therapeutic area medical strategy expert:

Internal:


Medical Affairs partners in therapeutic area

Global Medical Affairs Leadership

Marketing

Market Access

Clinical

Statistics

Translational Research

Regulatory Affairs

Project Leadership


External:


Investigators, KOLs

Global steering committees

Scientific Advisory Boards

Advocacy groups

Cooperative groups


The ideal candidate will have the following mix of professional and personal characteristics:


MD or MD, PhD preferably board certified in Hematology/Oncology.





A minimum of 7-10 years academic/industry experience strongly preferred.





Expertise in the conduct of clinical trials in hematology/oncology.





Excellent analytical skills and solid experience in translating medical/clinical information into medical affairs strategies.





Proficiency in critical data review and interpretation.





Matrix leadership of cross-functional teams.





Excellent oral and written communication skills, including presentations to large groups, facilitation of interactive discussions, and 1:1 discussions with thought leaders.





Demonstrated customer focus orientation & credibility with customers.





Knowledge/application of data sources, reports and tools for the creation of solid plans.





Regular travel will be required as needed


Bristol-Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees the resources to pursue their goals, both at work and in their personal lives.

Bristol-Myers Squibb is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

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