Medical Affairs Manager

Medical Affairs Manager, US (Oncology, Endocrinology, Radiopharmaceuticals)

Location: Hybrid - NYC or MA

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.