Curaclin Research has announced a new hiring opportunity for the position of Clinical Trial Assistant (CTA) in Bhubaneswar, Odisha. Candidates with 6 months to 2 years of experience in clinical research are encouraged to apply. This is an excellent opportunity for professionals looking to build a rewarding career in clinical trials, regulatory affairs, Trial Master File (TMF) management, and Good Clinical Practice (GCP).
If you have experience handling Ethics Committee (EC) submissions, regulatory documentation, and clinical trial coordination, this Curaclin Research Clinical Trial Assistant job could be your next career move.
Job Details
| Particular | Details |
|---|---|
| Company | Curaclin Research |
| Position | Clinical Trial Assistant (CTA) |
| Job Location | Bhubaneswar, Odisha |
| Experience | 6 Months – 2 Years |
| Employment Type | Full-Time |
| Industry | Clinical Research |
| Department | Clinical Operations |
Key Responsibilities
The selected Clinical Trial Assistant (CTA) will be responsible for:
- Handle Regulatory and Ethics Committee (EC) documentation.
- Prepare, submit, track, and follow up on regulatory and EC submissions.
- Maintain and update the Trial Master File (TMF) in compliance with Sponsor, ICH, and GCP guidelines.
- Coordinate with investigational sites for timely collection of essential study documents.
- Support study start-up activities, including site feasibility and activation readiness.
- Assist in protocol amendments, renewals, and regulatory submissions.
- Ensure clinical trial documentation complies with applicable regulatory requirements.
- Maintain accurate documentation throughout the clinical trial lifecycle.
Qualifications
Candidates should have:
- Bachelor’s degree in Life Sciences, Pharmacy, Clinical Research, or a related discipline.
- 6 months to 2 years of relevant experience in Clinical Research.
- Knowledge of:
- Good Clinical Practice (GCP)
- ICH Guidelines
- Trial Master File (TMF)
- Regulatory documentation
- Ethics Committee submissions
- Good communication and documentation skills.
- Strong organizational and coordination abilities.
Why Join Curaclin Research?
Working as a Clinical Trial Assistant at Curaclin Research offers:
- Opportunity to work on clinical research projects.
- Hands-on experience with regulatory documentation.
- Exposure to Sponsor and ICH-GCP compliant clinical trials.
- Career growth in Clinical Operations.
- Collaborative work environment.
- Professional development opportunities.
How to Apply
Interested candidates can send their updated resume to:
Email: hr@curaclinsmo.com
Job Location:
Bhubaneswar, Odisha
