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Clinical Trial Associate

1-3 Years
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  • Posted 12 days ago
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Job Description

  • Perform activities in compliance with corporate and clinical operations policies, SOPs, and work instructions.
  • Assist Clinical Monitoring staff with site management activities; act as a Sponsor representative for assigned studies.
  • Ensure sites comply with protocol requirements, study procedures, and relevant guidelines.
  • Create and maintain Trial Master File (TMF) and project files, including participation in audits.
  • Prepare and maintain site manuals, reference tools, and other study documents.
  • Maintain, update, and input clinical tracking information into databases.
  • Track incoming and outgoing clinical and regulatory documents for investigator sites, studies, project teams, or clients.
  • Manage shared mailbox, process site requests, and route correspondence appropriately.
  • Coordinate ordering, packaging, shipping, and tracking of site supplies and materials.
  • Handle receipt, tracking, and disposition of Case Report Forms (CRFs) and queries as needed.
  • Stay updated on clinical research developments by completing assigned training.

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: 135565527