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Medical Affairs Manager

2 months ago

New York, United States Masis Professional Group Full time

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


*Candidate MUST live within a commutable distance by car or train to downtown NYC.


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.