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Clinical Trials

1-5 Years
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  • Posted 22 days ago
  • Over 50 applicants
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Job Description

  • Creating and writing trial protocols and presenting them to the steering committee.
  • Identifying, evaluating, and establishing trial sites, and closing sites after trial completion.
  • Training site staff on therapeutic areas, protocol requirements, proper source documentation, and case report form completion.
  • Liaising with ethics committees regarding the rights, safety, and well-being of trial subjects.
  • Ordering, tracking, and managing investigational products (IP) and trial materials.
  • Overseeing and documenting IP dispensing, inventory, and reconciliation.
  • Protecting subject confidentiality, updating their information, and verifying IP administration according to protocol.
  • Conducting regular site visits, coordinating project meetings, and preparing visit reports.
  • Implementing corrective action plans for underperforming sites.
  • Liaising with regulatory authorities as required.
  • Ensuring compliance with SOPs, local regulations, ICH, and GCP guidelines.
  • Performing other clinical research tasks and responsibilities as assigned.

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: 135563847

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