Clinical Research Associate Job Duties

By | July 1, 2010

Clinical Research Associate Duties

The job of a Clinical Research Associate is to guide the writing the clinical protocols and managing any internal and external governance processes if required. Your duties also comprises of interacting directly to the investigator site to run the trial level logistics making sure that the deal will be in accordance with the protocol and it will be accomplished as per the study timelines .

Duties of Clinical Research Associate

  • A Clinical Research Associate holds a very responsible position as he has to operate as the main line of communication between the investor and the sponsor.
  • You will have to verify that all the research employees, services and investigational products holds adequate qualifications and funds and ensure that they continue to be adequate throughout.
  • Take responsibility in safety measures and conduct the trail properly.
  • You will have to ensure that the investor is following the standard protocol along with all GCP procedures.
  • One of your chief duties will be to verify that documents or source data as well as the other trial records are accomplished accurate and properly maintained.
  • Any unpleasant incident, concomitant medication or inter current diseases are report in line with the procedure on the CRFs.
  • Work as a team with the clinical pharmacologist as well as the statistician, pharmacokinetics and investigator in order to elaborate the study design and protocol development.

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