Reference: 10 23/04/2021 12:47:08

Director of Clinical Trial Management.

Cincinnati - United States $150,000-$200,000 Dependent on Experience

**SIGN ON BONUS ELIGIBLE**REMOTE OPTIONS AVAILABLE**COMPETITIVE BENEFITS**

Charlton Morris are partnered with a mid-sized CRO currently undergoing a huge expansion period within their Project Management/Clinical Operations department. They are currently seeking a Director of Clinical Trial Management, can be remote but office based preferred.

Below is the advert for Project Manager – Associate Director level, with an extension of Director level additional responsibilities:

Responsibilities:

  • Management and accountability of daily project operations, as stated by contract and regulations
  • Primary sponsor contact
  • Provide cross functional oversight of internal team, monitoring training needs
  • Maintain knowledge of protocol, therapeutic area and indication
  • Review and improvement to project documentation and project plans
  • Management of study vendors
  • Site management and CRA monitoring

**Benefits:**

  • Competitive salary package
  • Sign on bonus eligible
  • Remote working (5+ years experience)
  • Part of a forward thinking and competitive organisation, undergoing exciting expansion
  • Great progression opportunities

Requirements:

  • Bachelors degree in related field, advanced degree in related field
  • Phase 1-4 experience – SPECIFICALLY 2-3
  • 5 years of experience to qualify for remote working
  • Bid defense experience preferred

Additional Director info:

Unlike other CROs, their structure allows the clinical trial management team to focus on operational execution of the project, with minimal involvement in the P/L of project. This position will provide leadership to a team of Clinical Trial Managers as well as acting as a project director and being directly involved in client relationships and program oversight.

Responsibilities:

  • Lead a team of Clinical Trial Managers as a member of the global clinical operations management team
  • Represent the function in Business Development opportunities, including review of proposals and participation in key client meetings
  • Lead key global programs and operations as contact for the clients on strategic programs

Requirements:

  • Minimum of Bachelor’s degree; Master's degree or PhD preferred;
  • A minimum of 10 years’ experience in the clinical research industry, with at least 5 years' experience in clinical trial management (preferably with a CRO)

To apply directly – follow the link or email directly at Elisabeth.edmonds@lifesci-cm.com

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Consultant.

Elisabeth Edmonds
Elisabeth Edmonds
Business Consultant View Profile

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