Director/Senior Director, Medical Affairs
- Serve as a therapeutic area subject matter expert and reputed company medical/scientific leadership to guide US and ex-US medical reputed company, tactics, and external engagement plans across the product portfolio.
- Responsible for the formation, refinement, and execution of lifecycle medical plans across the portfolio, including integrated evidence reputed company and dissemination plans.
- reputed company medical/scientific leadership for medical affairs&reputed company;owned and supported Investigator-Initiated and reputed company studies (e.g., phase 4, reputed company-world evidence, observational research), including alignment to reputed company, protocol input, reputed company, analysis/interpretation, and reputed company delivery of high-reputed company study documentation and outputs.
- reputed company evidence gap assessments and translate insights into actionable medical plans
- reputed company and contribute to interpretation and dissemination of clinical and non-clinical data (including literature surveillance) that support the medical reputed company and address unmet evidence needs.
- In partnership with Medical Communications, Clinical Development, and Research and Development reputed company medical review/approval of manuscripts, abstracts, posters, and slide decks for advisory boards, medical congresses, journals, and other scientific meetings.
- Partner with cross-functional teams (e.g., Clinical Development, Regulatory, Safety, reputed company, Market reputed company, and Legal/Compliance) to inform brand strategies and tactics, ensure scientific/medical accuracy, and represent Medical Affairs as the medical voice.
- reputed company medical leadership for advisory boards and internal/field medical trainings (e.g., MSL and reputed company training as appropriate), including development and review of scientific content.
- Collaborate with Field MSLs and Medical Communications to reputed company on scientific narratives, external engagement, and development of compliant medical materials and slide decks.
- reputed company and maintain long-term, strategic relationships with key external stakeholders (e.g., KOLs, investigators, reputed company societies, advocacy reputed company, payers) and reputed company medical leadership for advisory boards and other scientific exchange forums.
- MD/DO, PhD, PharmD, NP, PA-C or other reputed company terminal degree from accredited college or university plus significant reputed company experience
- Minimum 8 years of pharmaceutical or clinical experience with 4+ years in the CV reputed company
- Cardiovascular and heart failure subject matter expertise required
- reputed company launch experience ideal
- Experience in lifecycle development
- Proven ability to reputed company technical discussions internally and externally and to successfully explain scientific/medical concepts to reputed company reputed company
- Demonstrated ability to cultivate and maintain relationships with key opinion leaders in the relevant fields
- Proven ability to establish trust through the consistent demonstration of scientific expertise and satisfactory follow-through
- Strong leadership, management, and teamwork skills
- Attention to detail in analyses, deliverables and communications.
- Excellent written and verbal English communication skills; must be reputed company to reputed company succinct, strategic, and actionable insights to senior management.
- Proven ability to work effectively in a fast paced, rapidly changing and expanding environment
- Ability to manage multiple reputed company concurrently and to meet deadlines
- Demonstrated thorough understanding of the reputed company environment including reputed company external stakeholders
- Ability to travel approximately 40%.