Responsibilities will include, but are not limited to, the following:
- Assist US Disease Lead with their responsibilities as part of a Global Franchise Team
- May 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
- Collaborate with Medical Affairs colleagues to guide and execute therapeutic area strategy and tactics with appropriate use of resources and performance to goals
- Support/may lead Medical Affairs cross-functional working groups
- May represent company at professional meetings, congresses, and local symposia.
- Provide assistance in the planning and execution of Medical Affairs Sponsored Trials, within appropriate standards for compliance, quality, timeliness, and budget. Support the Disease Leads in the design, execution, medical monitoring and evaluation of clinical trials according to strategy and good clinical practice.
- High quality scientific/clinical input and review of: Disease strategy/plans, abstracts, posters, slides, manuscripts in disease area, educational materials in disease area including slides, webcasts, etc., LOIs/ IIT protocols in disease area, steering committee and advisory board meeting objectives, materials, CTB, booth panels, Med info letters, CDPs, Commercial Brand plans, Integrated Disease Plans, ORQs in disease area, Scientific educational grant requests and patient advocacy grant requests
- Assist with Global and US Disease Strategy and Plans
- Track priority Medical Affairs tactics and performance to goals/budget
- Perform, as needed, research and analytics and provide recommendations to support quality medical decisions regarding clinical research, consultancy, and internal planning.
- May partner with Scientific Communications on developing publication strategy, gap analysis, and key messages
- Assist with scientific searches, data summaries, preparation for site visits/corporate visits/payor presentations
- Interaction with key stakeholders, as a therapeutic area and strategic expert:

Internal:
- Medical Affairs partners in therapeutic area
- Global Medical Affairs Leadership
- Marketing
- Market Access
- Clinical
- Statistics
- Translational Research
- Regulatory Affairs
- Project Leadership

External:
- Investigators, KOLs
- Global steering committees
- Scientific Advisory Boards
- Advocacy groups
- Cooperative groups

The ideal candidate will have the following mix of professional and personal characteristics:
- Advanced degree (Doctorate or Master’s) in health related field.
- Expertise in hematology/oncology including relevant content area, with 3+ 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.
- Product lifecycle management experience preferred.
- Good understanding of Medical Affairs and the compliance issues concerning MA function.
- Influence management of successful cross-functional and multi-disciplinary teams.
- Excellent communication and organization skills. Excellent presentation skills, including presenting to large groups, facilitation of interactive discussions, and 1:1 discussions with experts in the therapeutic area.
- Demonstrated customer focus orientation & credibility with customers.
- Knowledge/application of data sources, reports and tools for the creation of solid plans.
- Possess strong business acumen and financial skills. Budget experience.
- Regular travel will be required.

Qualifications
Advanced degree (Master’s or Doctorate) in health-related field. Expertise in hematology/oncology including relevant content area, with 3+ years industry experience, including expertise in the conduct of clinical trials in hematology/oncology.