Director Global Medical Affairs Oncology

Bristol Myers Squibb · Boudry - CH

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. 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.

Position Summary

Reporting to the Senior Director Multiple Myeloma (MM), this position provides scientific/medical leadership and strategic support for MM therapies in various stages of clinical development and will be responsible for the provision of strategic input as well as specific activities in relation to the design and delivery of a comprehensive Medical Affairs program for the therapy area Disease Team.

This individual will take a leadership role for the definition, execution and implementation of the Medical Affairs strategy in support of multiple myeloma CELMoD assets, representation on relevant cross-functional teams, and collaboration with the global affiliates. A major focus will be the interaction and alignment with Global functions (Medical Affairs and cross-functional) and the support to Medical Affairs functions in the global affiliates. The position 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. It may take a leadership role for the execution of medical affairs research and assist in the evaluation and support of investigator-initiated trials in their therapeutic area.  

As active member of WW cross-functional MM Team and other sub-teams and project groups, the position will be actively involved in cross-functional team activity, strategic and budget planning and other Medical Affairs functions supporting the business, as deemed appropriate.

Key Responsibilities

  • In collaboration with Senior Director, develop, design and execute the global therapeutic area strategy for multiple myeloma CELMoD assets and tactics consistent with global disease strategy
  • Lead the execution and implementation of the medical affairs plan, delivering the planned tactics and acting as the point of contact for global affiliates
  • Development and approval of medical and educational materials
  • Develop and assist with global and regional Disease Strategy
  • Support the design and planning of medical data generation (Investigator Sponsored Research, medical affairs sponsored trials, etc…)
  • Collaboration with the senior members of the MM MA Team in managing relations/communication with external Key Opinion Leaders and cooperative groups for external educational event opportunities at international symposium and stand-alone events
  • Contribution to central Key Opinion Leader management programs through organization and participation in Advisory- and Consultant meetings as appropriate.
  • Development and maintenance of assets integrated evidence plan, design and execution of initiatives.
  • Represent company at professional meetings and congresses
  • Represent Global Medical Affairs at key cross functional forums and teams (e.g. Clinical Development Team, Commercialization Team, Publication Team, etc) to provide disease area and product expertise
  • Collaboration with the respective cross-functional team, the clinical development and medical affairs groups to identify publication projects
  • Input into the central publication planning and publication review process. Seeking and initiating additional data exploration and managing the compilation and presentation of results with key stakeholders
  • Medical and scientific input on educational materials development and internal education program for WW colleagues
  • Management and collaboration with Medical Education & Communication agencies (vendors) to support delivery of events and materials
  • Management as appropriate of the budget allocated to the specific projects
  • Other responsibilities as assigned

Qualifications & Experience

  • Strong scientific background including a medical scientific degree (MS, PhD, MD) in medicine, molecular biology, genomics, cancer biology or other relevant life sciences area preferred, combined with 8+ years experience in clinical /translational research and medical affairs in hematology/oncology in academia/industry, experience in Multiple Myeloma desirable
  • Experience and knowledge of the drug development and/or commercialization process is essential
  • Proven track record of:
    • Delivering value in a highly professional Medical Affairs environment
    • Successful KOL relationship building and maintenance
    • Designing and planning educational event
    • Translating medical/clinical information and insights into medical affairs strategies

  • Excellent oral and written communication skills, including presentations to large groups, facilitation of interactive discussions, and 1:1 discussions with thought leaders
  • Proficiency in scientific and clinical data review and interpretation
  • Customer focus orientation & credibility with customers
  • Interest in internal training would be advantageous
  • Matrix leadership of cross-functional teams and strong organization skill with a can-do attitude
  • Ability to work productively in complex cross-cultural and cross functional teams 
  • Awareness of international diversity of clinical practices and healthcare systems
  • Strong identification with BMS’s values
  • Regular travel required (up to 30%)

If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.

Uniquely Interesting Work, Life-changing Careers
With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.

On-site Protocol

BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:

Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.

Supporting People with Disabilities

BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to [email protected]. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.

Candidate Rights

BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.

If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: https://careers.bms.com/california-residents/

Data Protection

We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at https://careers.bms.com/fraud-protection.

Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at [email protected]. Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley.

R1603296 : Director Global Medical Affairs Oncology

Healthcare pay context

Based on 3,320 disclosed Healthcare salaries on RoleSuite, the role pays a median of $116K/year, with most offers between $87K and $169K (10th–90th percentile: $66K–$250K).

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