Key Responsibilities - Scientific Engagement: Establish and maintain peer-to-peer relationships with key opinion leaders (KOLs), HCPs, and academic institutions to discuss scientific data, disease state education, and therapeutic insights.
- Medical Education: Deliver accurate and balanced scientific presentations to internal and external audiences, including at conferences, advisory boards, and educational events.
- Clinical Research Support: Collaborate with investigators on company-sponsored and investigator-initiated trials, providing medical and scientific support throughout the study lifecycle.
- Cross-Functional Collaboration: Work closely with internal teams such as Clinical Development, Regulatory Affairs, and Commercial to provide medical insights that inform strategic decisions.
- Compliance and Reporting: Ensure all activities comply with regulatory standards and company policies, and accurately document interactions and insights in the appropriate systems.
Qualifications - Education: Advanced degree (PharmD, PhD, MD, or equivalent) in a relevant scientific discipline.
- Experience: Minimum of 2 years in a field-based medical affairs role within the pharmaceutical, biotechnology, or medical device industry.
- Scientific Expertise: Deep understanding of therapeutic areas relevant to the company's portfolio, with the ability to interpret and communicate complex scientific data.
Preferred Qualifications - Familiarity with clinical trial processes and regulatory requirements.
- Proficiency in using CRM systems and digital communication tools.
This job description is a complete list of all desired skills, but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you!
