Executive Medical Director, Clinical Development (Oncology)

ExelixisKing of Prussia, PA
399d$323,000 - $458,500

About The Position

The Executive Medical Director, Clinical Development at Exelixis is responsible for leading and executing late-stage clinical trials for oncology products. This role involves designing clinical studies, interpreting results, and ensuring compliance with regulatory standards. The position requires collaboration with clinical teams, oversight of safety monitoring, and interaction with key opinion leaders in oncology.

Requirements

  • MD with board certification or eligibility in Oncology or Hematology/Oncology and 10 years post-residency related experience, or equivalent combination of education and experience.
  • Nine years of drug development experience in biotechnology or pharmaceutical industry, or a combination of academia and industry.
  • Hands-on experience in the design, execution, and reporting of controlled clinical trials in oncology.
  • Understanding of basic science relevant to clinical oncology (biochemistry, immunology, molecular biology and/or genetics).
  • Proven ability to effectively work in a cross-functional/matrix environment.
  • Strong interpersonal, influencing, presentation, and written and verbal communication skills.
  • Strong organizational and time management skills.

Nice To Haves

  • Experience with molecular targeted or immunological therapies in clinical oncology studies.

Responsibilities

  • Support the establishment of clinical trial strategies for oncology products in development.
  • Design, prepare and initiate study protocols and other required documentation in compliance with project plans, federal regulations, GCP and good medical practice.
  • Act as medical monitor for company sponsored trials.
  • Support project teams with therapeutic area specific information.
  • Collaborate with internal safety group in analyzing and reporting of safety data from clinical trials.
  • Analyze and interpret other clinical trial data and prepare reports for regulatory agencies and publication.
  • Interact with key opinion leaders and investigators in relevant disease specific area.
  • Ensure consistency of scientific and development strategies for oncology products in development.
  • Maintain the highest level of scientific and clinical knowledge in relevant disease specific area.

Benefits

  • 401k plan with generous company contributions
  • Group medical, dental and vision coverage
  • Life and disability insurance
  • Flexible spending accounts
  • Discretionary annual bonus program
  • Opportunity to purchase company stock
  • Long-term incentives
  • 15 accrued vacation days in the first year
  • 17 paid holidays including a company-wide winter shutdown in December
  • Up to 10 sick days throughout the calendar year

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What This Job Offers

Job Type

Full-time

Career Level

Senior

Industry

Professional, Scientific, and Technical Services

Education Level

Ph.D. or professional degree

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