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Clinical Project Manager/Associate Director Clinical Operations

Reference Number: 3734
Location: MA

Our client is a clinical-stage biotechnology company. They have asked us to assist them in their search for a Clinical Project Manager/Associate Director, Clinical Operations.

Major tasks and responsibilities will include:

  • Sets clear expectations. Monitors the deliverables of the CRO and external vendors to mitigate risk and fast track the data cleaning and end of study activities.
  • Monitors local site performance in relation to study timelines.
  • Oversees study deliverables, clinical trial budgets, and timelines to meet corporate objectives.
  • Works in collaboration with the Head of Clinical Operations.
  • Provides regular study status updates to senior management and proposes solutions for any issues, as necessary.
  • Assists with the development of monitoring guidelines.
  • Supervises site and investigator selection process.

We seek candidates with the following qualifications:

  • Requires a Bachelor’s degree in a scientific discipline or health related field .
  • Must have 10+ years of clinical research experience, preferably in industry (Pharma/ Biotech).
  • Requires 2+ years of experience working as a Clinical Project Manager or Clinical Trial Manager, and expert knowledge of planning and managing clinical program budgets.
  • Proficiency in Microsoft Project required.
  • Must have extensive experience managing multiple vendors, CROs, and complex protocols.
  • Requires understanding of drug development and program management from pre-IND through NDA.
  • Experience in early phase Oncology is required.

If interested, please email your resume as a Word attachment to us, reference 3734.  No calls or faxes, please. Include your daytime phone number and we will contact you confidentially or reply to your email.

Fairway Consulting Group is included in Hunt Scanlon’s list of Top 50 Healthcare & Life Sciences Search Firms.