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Vice President, Endocrinology (MD)


  • Manage Phase 2 and, if successful, Phase 3 clinical program in Cushing’s Syndrome
  • Key member of the clinical/regulatory leadership of the company
  • Provide medical input into product development strategies
  • Serve as medical monitor for clinical trials
  • Development strong working relationships with clinical investigators and experts
  • Develop clinical protocols
  • Review and interpret clinical data
  • Prepare clinical sections of regulatory documents
  • Assist in the identification of new product opportunities
  • Operate within Compliance Guidelines at all times


  • MD in medical endocrinology or relevant field, preferred
  • 5+ years of clinical development within endocrinology/diabetes in pharma, biotech, or large academic centers
  • Track record of leading at least 1 Phase 3 trial; major contribution to the clinical section of an NDA preferred
  • Deep knowledge of and experience in clinical trial methodology and clinical development strategy across all development stages
  • Experience in designing, conducting and analyzing clinical studies ranging from Phase 1 to Phase 3
  • Thorough understanding of the regulatory environment.
  • Experience in contribution to IND and NDA submissions
  • Excellent communications skills, both verbally and in writing
  • Able to build strong working relationships with medical experts in multiple therapeutic areas

If you are interested, please submit your resume by email to

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