Contract Medical Director


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Our client is seeking a Medical Director!

Our client is a clinical stage biopharmaceutical company that specializes in transient cardiovascular conditions. The Medical Director will play a leading role in the launch of a new therapy for the treatment of a common cardiovascular condition that currently has no FDA-approved therapies. This will be a contract opportunity throughout the duration of the clinical trial.

Specific Responsibilities:

  • Review study reports, subject narratives, and periodic safety reports
  • Provide medical oversight regarding protocol exemptions, protocol violations, protocol eligibility issues, concomitant medications, and general medical-related study issues
  • Respond to safety questions from the site or local IRB/IEC
  • Conduct medical training for the project team concerning study design and procedures
  • Review laboratory alerts, ECGs, Holters, and coordinate appropriate follow-up with study site and outside partners


  • MD required – cardiologist preferred
  • 3+ years of biopharmaceutical experience
  • Extensive experience in clinical research, clinical development, clinical judgment, & clinical data stewardship