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Medical Affairs Manager
2 months ago
Medical Affairs Manager, US (Oncology, Endocrinology, Radiopharmaceuticals)
*Candidate MUST live a within a commutable distance to Wilmington, MA. Hybrid is a must.
Company Overview:
Join a small but groundbreaking radiopharmaceutical development organization that retains its start-up spirit and is deeply committed to advancing patient care and developing new radiodiagnostic and radioligand therapy. They are currently seeking a highly skilled and motivated individual to fill the position of US Medical Affairs Manager with expertise in the therapeutic areas of oncology, or endocrinology, or radiopharmaceuticals.
Responsibilities:
Clinical Expertise:
- Serve as a key medical affairs representative, providing deep therapeutic knowledge in oncology, endocrinology, or radiopharmaceuticals.
- Stay abreast of the latest developments, clinical trials, and emerging trends within the specified therapeutic areas.
Scientific Communication:
- Collaborate with cross-functional teams to develop and communicate scientific and medical information to internal and external stakeholders.
- Create of educational materials, presentations, meetings and assist in publications to support the understanding of our products.
- Analysis of new indications and literature reviews of selected clinical topics.
KOL and Stakeholder Engagement:
- Identify, establish and maintain relationships with key opinion leaders (KOLs) and healthcare professionals in the specified therapeutic areas.
- Investigator Meetings, Advisory boards.
- Site identification and engagement of relevant KOL participants in clinical trial program, especially for the first indication of primary aldosteronism differential diagnosis.
- Organize and participate in advisory boards, symposia, and other scientific forums to gather insights and share information.
- Engage with indication-specific patient associations and guideline committees.
Regulatory Compliance:
- Ensure compliance with relevant regulations and industry standards in all medical affairs activities.
- Provide medical input into regulatory submissions and support interactions with regulatory agencies.
Cross-functional collaborations and contributions:
- Support early market access activities.
- Interacts and supports Phase 3 Clinical Development & Operations Team.
- Collaborate with internal teams, including EU medical Affairs, and US/ EU clinical development, to integrate medical strategies into overall business plans.
- Act as a medical resource for the business development team providing medical information and support as needed.
Qualifications:
- Medical Doctor (MD), or PhD in a relevant scientific field.
- Minimum 3 years of experience in medical affairs, medical liaison within the pharmaceutical or biotech industry.
- Demonstrated expertise in oncology, endocrinology, and/or radiopharmaceuticals.
- Strong understanding of clinical trial design and interpretation of clinical and scientific data.
- Excellent communication and presentation skills, with the ability to convey complex scientific information to diverse audiences.
- Proven ability to establish and maintain relationships with key opinion leaders.
- Strong organization skills and high degree of independence.
- Flexibility to travel across the US to interact with clinical and scientific though leaders.