Associate Director, US Medical, Lymphoma/CLL-Cell Therapy

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.

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 with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us.

The Associate Scientific Director, US Medical will report to the Senior Scientific Director, US Medical Lymphoma/Cell Therapy, provide scientific/medical leadership and support for lymphoma/Cell Therapy assets in various stages of clinical development.  This individual will take a leadership role for the execution and implementation of the Medical Strategy in support of lymphoma/CLL Cell Therapy assets, as well as representation on relevant cross-functional teams, and collaboration with the global affiliates. They may take a leadership role for the execution of medical affairs research and will also assist in the evaluation and support of investigator-initiated trials in their therapeutic area. He/she will serve as a therapeutic area expert in content creation, strategic and tactical discussions, and presentations with internal colleagues, as well as external experts and investigators.  He or She will also assist in leading pan-Cell Therapy activities including tactics to support the Cell Therapy franchise

Key Responsibilities       

• Collaborate with Medical Affairs colleagues to guide and execute therapeutic area strategy and tactics with appropriate use of resources.

• Assist Director on behalf of the Director/Disease Lead as a therapeutic area expert in both internal and external venues including the Medical Affairs sub-teams, and advisory boards / steering committees /ad counsels. 

• Support various Medical Affairs cross-functional working groups. 

• Assist with Cell Therapy site on boarding activities with Field Medical.

• Represent BMS at professional meetings, congresses, and local symposia.

• Support the planning and execution of Medical Affairs Sponsored Trials (MAST) and registries (as needed), within appropriate standards for compliance, quality, timeliness, and budget.

• Provide high quality scientific/clinical input and review of disease strategy plans, abstracts, posters, slides, manuscripts, educational materials, webcasts, IIT protocols, Commercial Brand plans, Scientific educational grant requests and patient advocacy grant requests. 

• Track priority Medical Affairs tactics and performance to goals/budget.

• Partner with Scientific Communications on developing publication strategy, data gap analysis, and key messages.

• Assist with scientific searches, data summaries, preparation for site visits/corporate visits/payor presentations Interaction with key stakeholders, as a scientific and strategic expert.

• Support medical information requests from field and work with medical field teams to develop appropriate responses and corresponding materials needed

• Assist in supporting the PAN-Cell Therapy tactics and tools including presentations, KOL engagements, and publications for the franchise

Qualifications and Experience

• Advanced degree (MS, PhD, MD) in medicine, molecular biology, genomics, cancer biology or other relevant life sciences area preferred.

• Experience in clinical /translational research and/or medical affairs in hematology or oncology with 5+ years industry experience. Master’s degree holders with 5+ years relevant industry experience may also apply.

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

• Proficiency in scientific and clinical data review and interpretation.

• Matrix leadership of cross-functional teams and strong organization skills.

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