Medical Director

1 week ago


Cambridge, Massachusetts, United States Relay Therapeutics Full time
Job Title: Vice President of Medical Affairs

Relay Therapeutics is seeking a highly skilled and experienced Vice President of Medical Affairs to lead our clinical-stage breast cancer program. As a key member of our team, you will be responsible for defining and implementing all aspects of clinical trial engagement and awareness.

Key Responsibilities:
  • Develop and execute an integrated Medical Affairs strategy with internal and external stakeholders, KOLs, clinical sites, and patients.
  • Establish and maintain credible scientific interactions with national and top regional opinion leaders, clinicians, and researchers in breast cancer.
  • Provide leadership with congress planning and key opinion leader engagement, including proactive facilitation of thought leader interactions and comprehensive review and presentation of key insights and feedback.
  • Plan and conduct Medical Advisory boards in collaboration with external agencies to obtain critical feedback/input on Relay Tx's breast cancer trial.
  • Partner with breast cancer advocacy groups to evaluate communication materials and raise awareness of Relay Tx clinical trials.
Requirements:
  • Health sciences advanced or doctoral degree, such as a PharmD, MD, or PhD, highly preferred.
  • PA, MSN, NP, DNP accompanied by previous pharmaceutical industry or clinical research experience in the area of breast cancer will be considered.
  • Clinical or prior pharmaceutical industry experience in the therapeutic area of oncology is required.
  • 10+ years of clinical or pharmaceutical experience with a minimum of 8 years of experience in field medical or clinical trial engagement and awareness roles.
  • Understanding of local medical practice and clinical decision-making as it pertains to patient care.
  • Ability to interpret scientific data and translate this information to meet educational, clinical, and research needs.
  • Ability and willingness to travel.
  • History of building long-term relationships with investigative sites, advocacy groups, and other key clinical research stakeholders.
  • Familiarity with effective digital clinical trials communication technologies.

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