Designation: Clinical Research Associate

Department: Clinical Trials

Qualification: M.Sc, B.Pharma, M. Pharma, Others

Experience: Min: 1 Year(s) - Max: 3 Year(s)

Primary Skills
Site Initiation
Feasibility and Site Selection
Valuable presentation skill
Site Close-out
Positive communication and documentation skills

Location

Cliantha Corporate

Responsibilities
Conduct SQV, SIV, monitoring, and close-out visits.
Ensure GCP, protocol, and regulatory compliance.
Review informed consent, safety reporting, and IP accountability.
Prepare timely and quality MVRs.
Maintain TMF/eTMF and essential documents.
Train and support site staff.
Ensure audit and inspection readiness.
Perform SDV/SDR and resolve data queries.
Monitor recruitment and site performance.
Escalate site issues and risks promptly.
Collaborate with study teams and stakeholders.
Manage monitoring schedules and site communication.

Disclaimer: This job posting and Location has been aggregated from external source. Role details, content, and availability are subject to change. Applicants are advised to confirm the latest information directly on the company website before applying.

📌 Clinical Research Associate Ahmedabad
🏢 Cliantha Research
📍 Ahmedabad