8 - 13 years

8 - 12 Lacs

Posted:6 days ago| Platform: Naukri logo

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Job Type

Full Time

Job Description

Key Responsibilities

  • Design, plan, and oversee clinical trials from initiation to closeout
  • Develop study protocols, informed consent forms, and case report forms
  • Ensure compliance with GCP, ICH, and local regulatory guidelines
  • Manage trial budgets, timelines, and resources
  • Coordinate with CROs, investigators, and ethics committees
  • Monitor trial progress and resolve operational issues
  • Review and analyze clinical data for accuracy and integrity
  • Prepare reports and presentations for internal and external stakeholders
  • Train and mentor clinical research staff
  • Support regulatory submissions and audits

Qualifications & Skills

  • M.Pharm / M.Sc / MBBS / MD in Life Sciences, Pharmacy, or Medicine
  • 8-12 years of experience in clinical research, with at least 3 years in a managerial role
  • Strong knowledge of clinical trial design, GCP, and regulatory frameworks

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