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Clinical Research associate

3-5 Years
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  • Posted 6 days ago
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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.

More Info

Job Type:
Employment Type:
Open to candidates from:
Indian

About Company

Seven Consultancy is a result of the motivation of young entrepreneurship under the guidance of experienced professional from industry. Young entrepreneurs know the recent trends of market. Flexibility of the services has helped Seven consultancy to secure a brand name in the market. So we have access to an overall career solution. Seven consultancy believes in shaping the way of success for its clients. Journey of Seven Consultancy started in 2007. Now it has crossed many milestones and added so many feathers in its crown. Currently operating from Kolkata & Mumbai to provide services all over India & abroad.

Job ID: 135564903

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