Clinical Research Coordinator

0 years

0 Lacs

Posted:5 days ago| Platform: Linkedin logo

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On-site

Job Type

Contractual

Job Description

About the Job

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Position Details

Role:

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Employment Type

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Key Responsibilities

  • Conduct clinical trials in compliance with ICH GCP and protocol guidelines.
  • Support study start-up activities and assist with site initiation.
  • Participate in recruitment and retention of study subjects.
  • Complete and maintain source documents, CRFs, and logs accurately.
  • Compile and update the Site Master File.
  • Manage Investigational Products (IP), including accountability and shipping.
  • Coordinate submissions and communication with the Ethics Committee.
  • Update sponsors on study progress and prepare for monitoring visits.
  • Perform other responsibilities assigned by management.


Who Can Apply

  • Freshers with a completed Clinical Research course.
  • Graduates/postgraduates in Life Sciences, Pharmacy, Biotechnology, or related fields.
  • Strong interest in clinical trials and regulatory compliance.
  • Excellent organisational, communication, and documentation skills.


Why Join Us?

🌟

🌟 Learn directly from experienced professionals.

🌟 Be part of innovative projects that shape the future of healthcare.

🌟 A great opportunity to grow your career in clinical research.

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