Interim Clinical Research Manager, phase III

Main responsibilities:

• Drive planning, execution and oversight of the company’s sponsored clinical trials (phase III).
• Has a comprehensive overview of all sponsored clinical study activities.
• Lead and document cross-functional study team and subsequent meetings from start-up through close out.
• Delegates study activities to project team as applicable. Identify process gaps,
  contribute on development of SOPs/working procedures as appropriate.
• Reports to Head of Clinical Operations on overall clinical trial progress.
• Supports other functions with identification of potential vendors and review of vendor
  information, proposal and bid defense presentations.
• Active Management and oversight of CRO during the course of the study.
• Review and approval selection of investigator site according to predefined criteria.
• Ensures the specific procedures, manuals and plans are developed, as needed.

To be considered for this role:

• 5-10 years of clinical trial management, requirered experience in global phase III pivotal trials, most preferably from a smaller life science company/head quarters. 
• Strong background in the operational aspects of clinical research trials Experience of working with oversight of outsourced sponsored clinical trials.
• Ability to review, interpret, and analyze information to support discussions and make
  decisions.
• Scientific/healthcare related degree preferred.
• Experience overseeing Service providers .
• Excellent interpersonal skills.

About the process:

This is a full-time assignment, starting latest mid August. The assignment is expected to last 6-9 months. The client would appreciate if the consultant is open to a permanent position after the interim period. Candidate presentations will take place latest beginning of July. Do you have the right profile and availability? Apply today!