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
- Positive presentation skill
- Site Close-out
- Good 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.

Role: Clinical research Scientist, Industry Type: Clinical Research / Contract Research, Department: Research & Development, Employment Type: Full Time, Permanent Role Category: Pharmaceutical & Biotechnology Education UG: Any Graduate PG: Any Postgraduate Key Skills clinical researchclinical trialscomplianceetmfgcppharmaregulatory complianceresearchsite initiation

📌 Clinical Research Associate (Ahmedabad)
🏢 Cliantha Research
📍 Ahmedabad