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Post : Clinical Research Associate
Job Description
The associate monitors trial sites, checks that studies follow the protocol and good clinical practice, and keeps data and records reliable. The hospitals host investigator-led and sponsored studies, and the associate supports their site teams.
What the associate handles
• Carry out site initiation, monitoring and close-out activities as assigned
• Verify data against source documents and resolve queries
• Check compliance with the protocol, ICH-GCP and local regulations
• Review informed-consent and safety-reporting processes
• Maintain trial master file documents and site files
• Write monitoring visit reports and follow up on actions
• Support investigators and site staff with training and questions
Candidate Profile
• 2 to 6 years in clinical trial monitoring or clinical operations
• Bachelor's or master's degree in life sciences, pharmacy or medicine
• Experience in clinical monitoring or clinical operations
• Working knowledge of ICH-GCP and Indian clinical-trial regulations
• Careful documentation and good attention to detail
• Willingness to travel to sites
Additional strengths
• Experience with an eTMF or EDC system
• Therapeutic experience in oncology, cardiology or diabetes
• Formal GCP certification
What the seat gives
• A Clinical Research Associate seat at a hospital group, reporting to the clinical project manager
• On-site in Delhi or Hyderabad, with a placement intended to be long term
• Varied trial exposure across sites and therapy areas
Additional Information
Experience : 2 to 6 years
Qualification : M.Pharm, B.Pharm, M.Sc, B.Sc
Location : Delhi or Hyderabad (on-site)
Industry Type : Pharma/ Healthcare/ Clinical research
End Date : 30th November 2025
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