drjobs Director, Clinical Research Operations العربية

Director, Clinical Research Operations

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Job Location drjobs

Menlo Park, CA - USA

Monthly Salary drjobs

Not Disclosed

drjobs

Salary Not Disclosed

Job Description

Our client seeks a Clinical Research Operations professional to plan their Phase I Clinical Trials

Requirements

  • Bachelors Degree in life sciences or healthcare field. Additional coursework in clinical trial design.

  • Ability to travel as required (up to 25%).

  • 12+ years of proven experience in clinical research and/or clinical trial operations, including a minimum of 7 years in a supervisory role managing (internal/external) clinical operations staff.

  • Industry experience within pharmaceutical and/or biologics and prior experience in FDA negotiations relating to the conduct of regulated clinical trials.

  • Comprehensive understanding of applicable clinical research regulations. Thorough knowledge of GCP, ICH guidelines and other US and international clinical regulatory requirements.

Day to Day Responsibilities

  • Oversee the companys Clinical Operations activities and implementation of clinical studies and development programs.

  • Ensure operational feasibility of clinical development plans, including timeline, budget and resource requirements.

  • Ensure that all activities are completed in accordance with ICH GCP regulations, health authority regulations and SOPs.

  • Set the direction of the Clinical Operation organization and lead strategic discussions regarding program and study resourcing.

  • Hire, supervise and train operations personnel and assume ownership of the quality of clinical deliverables.

  • Procure CRO and vendors and provide oversight throughout the life of all assigned activities. Ensure transparency for costs, deliverables and quality expectations.

  • Define patient recruitment strategies and ensure operational feasibility and timely implementation of the set study goals.

  • Work with other Medical/Clinical team members on study documents including clinical trial protocol and amendments, ICFs, CRFs, IND, IB, CRO contracts, study reports, etc.


Employment Type

Full Time

About Company

10 employees
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