Medical Director GMA Cambridge MA
Cambridge, MA 02141
Location: Cambridge, MA
Company: Top BioPharma Company
Compensation: $150,000 to $265,000 Base + Bonus + Stocks + Amazing Benefits
Contact: Ken Kupersmith - [email protected]
The Medical Director Global Medical Affairs (GMA) will provide strategic input/guidance into the development and execution of the medical strategy for Hemophilia Products. As the in-house scientific subject matter expert (SME), this individual will provide scientific and medical expertise and work in close collaboration with cross-functional colleagues in Regulatory, Market Access, Clinical Development, Commercial, Corporate Affairs and Patient Advocacy.
Responsibilities & Qualifications
1.MD, PhD, or other doctorate degree in the life sciences
2.Experience with Hemophilia
3.This position will be based in Cambridge, MA and applicants must be willing to relocate.
4.A strong leader with project management skills and strategic acumen including a flexible, hands-on nature that works with a high sense of urgency.
5.Provide scientific and medical leadership for hemophilia products, including development of strategic plans, calling out specific unmet medical needs, key data gaps for the products and opportunities to engage with key stakeholders.
6.Leading the design and execution of the hemophilia product medical plan and tactics including life cycle management and real world evidence generation plans in collaboration with the Medical Research group
7.As the SME provide disease area expertise and oversee the development of focused medical training and communication priorities for hemophilia products including; review abstracts, publications, medical information letters, training, statistical analysis and other medical or commercial documents for promotional or scientific use
8.Collaborate with Regional and/or Affiliate Medical to ensure regional activities are aligned with medical strategy and that key internal stakeholders are sufficiently aware of affiliate and regional insights and needs
9.Involvement with key HCPs in the exchange of scientific and medical information including Advisory Boards and presentations at national and international meetings
10.Develop and maintain close professional relationships with Key Opinion Leaders (KOLs - physicians, nurses, other treatment team members) and emerging scientific leaders in the community
11.5+ years of Pharmaceutical industry experience with relevant experience in Medical Affairs
12.Strong background in ethical evaluation of clinical research projects