Senior Director GMA Oncology
Northern NJ, NJ 07920
Location: Northern NJ
Company: Top BioPharma Company
Compensation: $200k to $260k Base + Bonus + Big Stocks + Amazing Benefits
Contact: Ken Kupersmith- [email protected]
New Oncology R&D Department at Major Pharmaceutical aims to deliver seven distinct new molecular entities over next eight years.
The Senior Director Global Medical Affairs (GMA) Oncology will be the leader for assigned compound(s) under the leadership of the GMA Franchise head. This position will develop the GMA strategy and execution of the Global Medical Affairs plans including Launch Readiness and Life cycle management.
1.Responsible for the development of the Global Medical Affairs strategy and execution of the GMA plans including evidence generation, scientific exchange and data communication. Leads Launch Readiness activities and life cycle management from a medical perspective
2.Lead or co-leads GMAT, to gain strategic and planning alignment across regions and functions. Member of Pub, clinical, safety, RWE sub teams, GBT, GPT including trials concept sheets.
3.Provides Medical leadership to Medical Study Teams for sponsored trials. Manages all medical aspects and drives execution for assigned GMA clinical trial projects in collaboration with other global line functions, assigned Clinical Trial Operation teams, and regional/country medical associates.
4.Medical support for market access discussions.
5.Leads review of investigator-initiated studies (IIS), within Global IIS review Committee, for assigned projects(s).
6.Provides input into and reviews abstracts, manuscripts, press releases, promotional materials, educational slide decks, medical response documents. Efficiently manage budgets and resources for Sponsored and GMA supported activities, in collaboration with GMA Franchise Head
1.MD, PhD, or PharmD Required, MD preferred
2.Advanced knowledge in medical/scientific Oncology required, excellent knowledge of current clinical practice.
3.Builds strong cross-functional and global relationships- Interacts with regions, MKT Access, HEOR, Brand team.
4.Have expert operational knowledge and experience in clinical trial design and all stages of clinical trial conduct (Trial design, Start-up, Execution, Analysis, Reporting).
5.Have strong knowledge in and understanding of medical activities (including scientific communications, medical information, MSLs, and HEOR), relating to the commercialization of oncology products.
6.More than 5 years experience in pharma GMA role.
7.Medical expertise to ensure successful product launches across functions and life cycle management
8.Provide training to external and internal customers as the Subject Matter Expert (SME)
9.Define publication strategy and contribute to publication planning
10.Integrate medical expertise with commercial perspective