Clinical Research Associate

• Assist in initiating, monitoring, and closing clinical trial sites under supervision.
• Ensure that clinical trial sites comply with study protocols and regulatory requirements.
• Support in maintaining communication with site investigators and coordinators.
• Review source documents and case report forms (CRFs) for accuracy and completeness.
• Assist in resolving data discrepancies and ensuring data quality.
• Maintain essential trial documents (Trial Master File).
• Ensure adherence to ICH-GCP, SOPs, and study-specific procedures.
• Support preparation of regulatory submissions and ethics committee documents.
• Coordinate between sponsors, clinical sites, and internal teams.
• Participate in investigator meetings and training sessions.

Job Types: Full-time, Permanent, Fresher

Pay: ₹24,893.05 - ₹42,084.20 per month

Benefits:

• Health insurance
• Paid sick time
• Provident Fund

Work Location: In person