Clinical Project Manager/Director, Clinical Operations

About this job

The Clinical Project Manager/Director, Clinical Operations (DCO) assists in the planning and execution of clinical trials while adhering to budget, scope and timelines.   The CPM/DCO is responsible for managing all aspects of a clinical trial or multiple clinical trials including vendor selection and management and oversight to ensure patient safety, adherence to the contract, protocol and appropriate safety regulations and data integrity.

Responsibilities

  • Lead planning and communication with cross-functional study teams to ensure proper execution and conduct of the trial.
  • Prepare, oversee, and review all study related documents including protocols, informed consent forms, vendor and site budget, etc.
  • Ensure compliance to SOPs
  • Organize and lead CRO/vendor meetings
  • Maintain study timelines
  • Provide updates to internal line functions and management team
  • Participate in the preparation, review, updating and training of SOPs

Minimal Experience and Skills

  • BS/BA, Master’s Degree Preferred
  • Preferred Major – Life Science
  • Candidates should have 8-10 years of relevant work experience

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