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Director, WW Medical Affairs Hematology, MM, CAR T cell therapy
View: 168
Update day: 08-04-2024
Location: Boudry Neuchâtel NE
Category: Health / Medical Care
Industry: Pharmaceutical Manufacturing
Position: Director
Job type: Full-time
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Job content
Working with UsChallenging. 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-usPosition SummaryReporting to the Senior Scientific Director Multiple Myeloma (MM), this position provides scientific/medical leadership and strategic support for MM CAR T cell 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 MM CAR T cell therapies as well as 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). This will be done through the active participation to a WW cross-functional team (MA, MKT and Market Access) where the position will contribute to the global strategy while co-leading the launch implementation and roll-over of new indications in key countries from a Medical Affairs perspective. This individual 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.The position will serve as a therapeutic area expert in strategic and tactical discussions, and presentations with internal colleagues, as well as external experts and investigators.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 and design the global therapeutic area strategy for MM CAR T cell therapies and tactics consistent with global disease strategy
- Develop and assist with global and regional Disease Strategy
- Provision of therapeutic area expertise in both internal and external venues including the Medical Affairs sub-teams, and advisory boards / steering committees
- In collaboration with senior director, provide expert matter support to the asset development project team
- Development and maintenance of assets integrated evidence plan, design and execution of initiatives to address the identified data gaps
- Support the design and planning of medical data generation (Investigator Sponsored Researchs, medical affairs sponsored trials, etc…)
- Contribution to central Key Opinion Leader management programs through organization and participation in Advisory- and Consultant meetings as appropriate.
- Represent company at professional meetings and congresses
- Represent Global Medical Affairs at key relevant cross functional forums and teams (e.g. Development Project Team, Worldwide Brand Team, Publication Team, etc) to provide disease area and product expertise
- Collaboration with cross-functional colleagues to agree, establish and recommend the priorities in the assigned area of responsibility within the asset strategy
- 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
- Management as appropriate of the budget allocated to the specific projects
- Other responsibilities as assigned
- 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 7+ years experience in clinical /translational research and medical affairs in hematology/oncology in academia/industry, experience in Multiple Myeloma desirable
- Experience and deep knowledge of the drug development and/or commercialization process is essential
- Proven track record of:
- Translating medical/clinical information and insights into medical affairs strategies
- Generating a comprehensive strategic medical plan
- Successful KOL relationship building and maintenance
- Excellent analytical skills and solid experience in translating medical/clinical information 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.
- Customer focus orientation & credibility with customers.
- 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%)
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Deadline: 23-05-2024
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