Curaclin Research Pvt. Ltd. has announced an excellent opportunity for aspiring clinical research professionals to join as a Clinical Trial Assistant (CTA) in Bhubaneswar, Odisha. This role is ideal for candidates with 6 months to 2 years of experience in clinical trials, regulatory documentation, and TMF management.
With increasing demand in the clinical research industry, Clinical Trial Assistant jobs in India are becoming a strong entry point for careers in CROs and SMOs. If you’re aiming to build expertise in ICH-GCP, regulatory submissions, and trial coordination, this opportunity is highly relevant.
📌 Job Overview
- Position: Clinical Trial Assistant (CTA – Post 2)
- Company: Curaclin Research Pvt. Ltd.
- Location: Bhubaneswar, Odisha
- Experience Required: 6 Months – 2 Years
- Job Type: Full-Time
- Open Positions: 2
- Preference: Immediate Joiners
🧪 Key Responsibilities
As a Clinical Trial Assistant, you will be responsible for supporting clinical operations and ensuring compliance with regulatory standards:
- Manage Regulatory & Ethics Committee (EC) submissions, tracking, and follow-ups
- Maintain and update Trial Master File (TMF) in compliance with ICH-GCP guidelines
- Coordinate with investigational sites for essential document collection
- Assist in study start-up activities, including feasibility and site activation
- Support protocol amendments, submissions, and renewals
- Ensure proper documentation aligned with clinical trial regulatory requirements
🎓 Qualifications & Skills
- Bachelor’s or Master’s degree in Life Sciences / Pharmacy / Clinical Research
- 6 months to 2 years of experience in clinical trial assistant roles or similar profiles
- Strong understanding of:
- ICH-GCP guidelines
- Regulatory submissions & EC processes
- Trial Master File (TMF) management
- Good communication and coordination skills
- Attention to detail and documentation accuracy
💼 Benefits of This Role
- Opportunity to work in a growing clinical research organization (CRO/SMO)
- Hands-on experience in clinical trial documentation and regulatory affairs
- Exposure to end-to-end clinical trial processes
- Career growth in clinical operations, CRA, and regulatory roles
📩 How to Apply
Interested and eligible candidates can apply by sending their updated CV to:
Make sure your resume highlights your experience in clinical trials, TMF, and regulatory documentation to improve your chances of selection.
