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Sr. Director, Medical Affairs, Lung and Head & Neck Cancer-(northern NJ)
Responsible for the planning and timely execution of Medical Affairs Sponsored Trials, within appropriate standards for compliance, quality, timeliness, and budget.
Represent US Medical Affairs on behalf of the Disease Lead as a therapeutic area expert in both internal and external venues including the Global Franchise Team, clinical sub-teams, and advisory boards / steering committees.
Lead/support various Medical Affairs cross-functional working groups.
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.
MD or MD,PhD board certified in Hematology/Oncology preferred. 7-10 years industry experience. 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. Knowledge/application of data sources, reports and tools for the creation of solid plans. Possess experience creating and managing budgets.