"Senior Director, ( MD) Global Development Lead, Early Development"
Pfizer
Senior Director, Medical Affairs
PharmaEssentia
full-time
Posted on:
Origin: • 🇺🇸 United States
Visit company websiteJob Level
Senior
About the role
- Identify and integrate the unmet needs and perspectives of healthcare providers, payers, patients, and caregivers into product and franchise Medical Affairs strategies
- Strategic development and overall accountability and tactical execution of our flagship product ropeginterferon launch in polycythemia vera
- Collaborate cross-functionally as well as collaborate with external KOLs and decision-makers
- Lead the PharmaEssentia platform and product portfolio specific Medical Affairs strategy and execution
- Develop, execute and collaborate a highly efficient, integrated US medical affairs/scientific strategy
- Provide management and oversight of the Medical Affairs team which includes the US HEOR team, publication and scientific communication team, call center, Congress planning and KOL mapping and strategy
- Scientific evidence generation (RWE, HEOR, Phase IV and IIT) and scientific information exchange with all key stakeholders
- Involvement in the planning, strategy, tactics, slide deck development, and training of the MSL team; strong collaboration with the MSL director
- Provide cross-functional support to MSLs, medical information, regulatory affairs and clinical development with medical and scientific expertise for life cycle management
- Review and approve medical and scientific content of Regulatory, Safety, Medical Affairs, and Commercial
- Partner with stakeholders to develop and implement real world evidence generating strategies for assigned programs and provide subject matter expertise
- Provide Strategic Guidance / US PEC representation at corporate meetings & events
- Serve as Launch Lead/MSL Lead; engage External Experts (Providers, Payers, Advocacy)
- Support Clinical Development and study-site engagement, and identify and manage relationships with key stakeholders
Requirements
- PhD or PharmD required; MD degree preferred
- Minimum of 10 years of relevant working experience in the Pharmaceutical/Biotechnology industry
- Minimum of 6 years of experience in Medical Affairs
- Ability to articulate complex scientific and medical information in understandable business terms
- Knowledgeable in regulatory guidelines and clinical terminology
- Ability to work independently and with a team with strong writing, communication, and project management skills
- Thorough understanding of clinical methodologies and providing sound analytical support, you quickly establish credibility as a reliable resource
- Experience developing engagement and education tools
- Clinical trial support experience
- Travel required - up to 25%
- Preferred: Experience in hematology/oncology and rare diseases
