CRA - Remote - Contract

South San Francisco  ‐ Onsite
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Description

In this role, the CRA is responsible for the timely production of high quality data, adhering to the standards set by the Company/Sponsor in the Standard Operating Procedures for clinical studies. The CRA, in concert with the Project Leader, is accountable for the timely, quality, satisfactory, and cost-effective completion of the client's study.

RESPONSIBILITIES
  • Identifies potential investigational sites
  • Coordinates and performs comprehensive site management, including ISF/TMF maintenance and site correspondence
  • Conducts pre-study, initiation, interim and close out monitoring visits
  • Produces comprehensive visit, status and telephone contact reports
  • Resolves data issues and audit issues
  • Adheres to study timelines and budget
  • Mentors other CRAs
  • Collects high quality essential documents and supports completion of ethics committee and regulatory submissions (if applicable per region)


EDUCATION/EXPERIENCE REQUIREMENTS:
  • Minimum of two-plus years regional monitoring experience (CRO and Pharma environment preferred)
  • A four-year degree, preferably in a life science, nursing, or related discipline
  • Clinical research experience in one or more of the therapeutic areas mentioned below
  • Located within 50 miles of a major airport.
  • Experience with Oncology, Device/Cardiac Device, or Dialysis is strongly preferred. Other complex therapeutic experience considered.
Start date
08/2014
From
Real Staffing
Published at
07.08.2014
Project ID:
754341
Contract type
Freelance
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