Clinical Research associate

2 - 5 years

4 - 7 Lacs

Posted:13 hours ago| Platform: Foundit logo

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Work Mode

On-site

Job Type

Full Time

Job Description

  • Create and write trial protocols and present them to the steering committee.
  • Identify, evaluate, and establish trial sites, and close sites upon trial completion.
  • Train site staff on therapeutic areas, protocol requirements, proper source documentation, and case report form completion.
  • Liaise with ethics committees regarding the rights, safety, and well-being of trial subjects.
  • Order, track, and manage investigational products (IP) and trial materials.
  • Oversee and document IP dispensing, inventory management, and reconciliation.
  • Protect subject confidentiality, update information, and verify that IP has been dispensed and administered according to protocol.
  • Conduct regular site visits, coordinate project meetings, and write visit reports.

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