? We’re Hiring | Clinical Research Associate (CRA)

Experience: 7+ Years
Cliniv is looking for an experienced and dedicated Clinical Research Associate (CRA) to join our growing team and contribute to the successful execution of clinical research studies.
? Key Responsibilities:
• Conduct clinical trial monitoring visits, including site initiation, routine monitoring, and close-out visits.
• Ensure compliance with study protocols, ICH-GCP guidelines, and applicable regulatory requirements.
• Perform Source Data Verification (SDV) and review clinical trial documentation.
• Monitor patient safety, data integrity, and protocol compliance.
• Coordinate with Principal Investigators, site coordinators, and other study personnel.
• Review essential documents and maintain Trial Master File (TMF) documentation.
• Identify, document, and follow up on protocol deviations, queries, and site-related issues.




• Prepare monitoring visit reports and ensure timely resolution of findings.

? Candidate Profile:
• Minimum 7+ years of experience in clinical research.
• Strong knowledge of clinical trial processes, monitoring, and GCP guidelines.
• Excellent communication, coordination, and documentation skills.
• Ability to manage multiple clinical sites and ensure study quality.

? Interested candidates: Please share your updated CV via direct message or email it to "[email protected]".
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📌 Clinical Research Associate (India)
🏢 Cliniv Health Tech
📍 India