Clinical Research Associate
Company: Cliniv Health Tech
- Location: Telangana, India
- Seniority: Entry level
- Employment type: Full-time
- Posted: 8 days ago
- Offer language: English
Job description
📢 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 "info@cliniv.in".
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