Position:
Regional Clinical Research Associate
Description/ Responsibilities:
  • Study management, site management of study projects at local clinical sites
  • Responsible for monitoring of study activities
  • Coordinate all study activities to ensure protocol and regulatory requirement(s) are met (e.g., sample collection, sample processing, clinic set-up, etc.)
  • Adverse Event and Serious Adverse Event reporting
  • GCP compliant documentation for every project
  • Maintain adequate, accurate, complete and legible records.
  • Responsible for remaining current with regulatory requirements (DRAP, TPD, FDA, EMEA, UK MHRA etc.)
  • To perform any other duties as required, as training and experience allow.
  • Will perform tasks as assigned by supervisor.
Qualifications:

Education : Medical Background ( MBBS / BDS / Pharm-D / Graduation in Health Sciences )

CCRP / GCP Certification or equivalent.

Employment Type
Full-time
Beginning of employment
8th August 2022
Industry
Clinical Research Organization
Job Location
Lahore , Pakistan
Date posted
July 21, 2022
Valid through
July 26, 2022
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Position: Regional Clinical Research Associate

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