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Search for Jobs by Sheryl Horowitz

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Clinical Trial Associate - CTA (Science & Biotech)
Durham , NC 27701
Recruited by: Sheryl Horowitz | Owner | F-O-R-T-U-N-E Personnel Consultants, Inc. See all my Jobs

  • Hiring Company: F-O-R-T-U-N-E Personnel Consultants, Inc.
  • Industry: Science & Biotech
  • Compensation: Salary
  • Expires: Feb 09, 2020
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Job Description

The Clinical Trials Assistant (CTA) will support the clinical project team in the following areas: study start-up and site regulatory document collection; accurately update and maintain clinical systems within project timelines; prepare, handle, distribute, file, and archive clinical documentation and reports; review of study files periodically for accuracy and completeness; prepare, handle and distribution of Clinical Trial Supplies and maintenance of tracking information; track and manage Case Report Forms (CRFs), queries and clinical data flow. May act as a central contact for the clinical team for designated project communications, correspondence and associated documentation. Perform administrative tasks to support team members with clinical trial execution as needed.
Responsibilities Include:
Provide support to the Project Team throughout the conduct of clinical trials. Communicate and follow up on actions between clients, sites, and the project team and to be viewed by the CRAs and Project Managers as an important source of project information and assistance.
• Support the project team as needed.
• Assist with start-up activities to include site regulatory document collection.
• Update and maintain clinical systems within project timelines.
• Prepare, handle, distribute, file, and archive clinical documentation and reports.
• Review of study files periodically for accuracy and completeness.
• Prepare, handle and distribute of Clinical Trial Supplies and maintenance of tracking information.
• Track and manage Case Report Forms (CRFs), queries and clinical data flow. May act as a central contact for the clinical team for designated project communications, correspondence and associated documentation.
• Perform administrative tasks to support team members with clinical trial execution as needed.
• Assist sites with preparation for planned and unannounced audits with some guidance.
• Organize project meetings and taking of minutes.
• Maintain appropriate professional relationships utilizing an assertive, business-like manner which fosters study compliance.