Curaclin Research is actively hiring a Clinical Trial Assistant (CTA – Post 2) for its Bhubaneswar, Odisha location. This opportunity is ideal for candidates with 6 months to 2 years of experience in clinical research who are looking to build a strong career in regulatory affairs, ethics committee coordination, and TMF management.
If you are passionate about clinical trials, GCP compliance, and regulatory documentation, this role offers hands-on exposure across the clinical trial lifecycle—from study start-up to ongoing regulatory maintenance.
🏢 About Curaclin Research
Curaclin Research is a growing clinical research organization (CRO) engaged in supporting ethical, compliant, and high-quality clinical trials in line with ICH-GCP guidelines. The organization works closely with investigational sites, ethics committees, and sponsors to ensure regulatory excellence.
📌 Job Details
- Position: Clinical Trial Assistant (CTA – Post 2)
- Experience Required: 6 months to 2 years
- Location: Bhubaneswar, Odisha
- Employment Type: Full-time
- Industry: Clinical Research / CRO
🧾 Key Responsibilities – Clinical Trial Assistant
As a Clinical Trial Assistant at Curaclin Research, your responsibilities will include:
- Handling Regulatory and Ethics Committee (EC) documentation, submissions, tracking, and follow-ups
- Preparing and managing initial submissions, amendments, and renewals as per protocol requirements
- Maintaining and updating the Trial Master File (TMF) in compliance with ICH-GCP and sponsor guidelines
- Coordinating with investigational sites for timely collection of essential documents
- Supporting study start-up activities, including site feasibility, document collection, and site activation readiness
- Ensuring accurate documentation and audit readiness throughout the study lifecycle
Primary keywords used naturally: Clinical Trial Assistant job, CTA jobs in Bhubaneswar, Clinical Research jobs in Odisha
🎓 Qualifications & Skills Required
- Bachelor’s or Master’s degree in Pharmacy, Life Sciences, Biotechnology, or Clinical Research
- 6 months to 2 years of hands-on experience in clinical trial coordination or regulatory support
- Working knowledge of ICH-GCP guidelines, TMF, and EC submissions
- Strong documentation, coordination, and communication skills
- Attention to detail and ability to meet regulatory timelines
💼 Salary & Benefits
- Salary Range: ₹2,50,000 – ₹4,00,000 per annum (INR), depending on experience
- Exposure to end-to-end clinical trial processes
- Professional growth in regulatory affairs and clinical operations
- Opportunity to work closely with experienced clinical research professionals
📨 How to Apply – Curaclin Research CTA Job
Interested and eligible candidates can apply by sending their updated resume to:
📧 Email: hr.curaclinresearch@gmail.com
📍 Job Location: Bhubaneswar, Odisha
👉 Mention “Clinical Trial Assistant – Bhubaneswar” in the email subject line for faster screening.
