Job Description:

  • Prepare and review study-related documents i.e. Protocol, ICD, CRF, and all other relevant documents in accordance with regulatory compliance.
  • Records and Data compilations/Writings to support clinical study regulatory requirements needed for drug development and registration process.
  • Performing Project Coordination, Project Planning, and its execution and management

Location: Gandhinagar, Ahmedabad

Qualification: B.Pharma, M.Pharma

Experience: 2-5 Years

Salary: Negotiable

Contact Details:

Vilsha Shah



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