If you are looking for a Clinical Trial Assistant (CTA) job in Nagpur, this opportunity at HRAPL could be a strong career move. The organization is actively hiring experienced professionals to support clinical trial documentation, TMF management, and site coordination in compliance with global regulatory standards.
This role is ideal for candidates with 2–3 years of experience in clinical research who want to grow in clinical operations and contribute to quality-driven trial execution.
🔬 Job Overview
- Position: Clinical Trial Assistant (CTA)
- Company: HRAPL
- Location: Nagpur, Maharashtra
- Experience: 2–3 Years
- Qualification: Life Sciences / Pharmacy / Biotechnology Graduate or Postgraduate
- Employment Type: Full-Time
- Open Positions: 1
- Application Mode: Email
🧾 Key Responsibilities
As a Clinical Trial Assistant (CTA), you will:
- Support clinical trial documentation and regulatory compliance
- Maintain and update Trial Master File (TMF / eTMF)
- Assist in site coordination and communication
- Ensure adherence to ICH-GCP guidelines and SOPs
- Track study progress, documentation, and timelines
- Perform data tracking and documentation quality checks
- Collaborate with clinical teams for smooth trial execution
🎓 Eligibility Criteria
To qualify for this Clinical Trial Assistant job in Nagpur, candidates must have:
- Graduate/Postgraduate degree in:
- Life Sciences
- Pharmacy (B.Pharm / M.Pharm)
- Biotechnology or related field
- 2–3 years of experience as a CTA in clinical research
- Strong understanding of:
- Clinical trial processes
- ICH-GCP guidelines
- Proficiency in:
- MS Excel and documentation handling
- Good organizational and communication skills
- Ability to manage site coordination and data tracking
👉 Candidates from Nagpur are preferred.
💰 Salary (Estimated)
- ₹3.0 – ₹5.5 LPA (INR)
(Based on experience, role scope, and industry benchmarks for CTA roles in India)
🌟 Benefits
- Opportunity to work on regulated clinical trials
- Exposure to TMF, site management, and compliance processes
- Career growth in clinical operations and research
- Hands-on experience with documentation and audit readiness
- Stable role in a growing clinical research environment
📩 How to Apply
Interested candidates can apply via email:
- Email ID: contact@hrapl.in
- Subject Line: Name_CTA
Ensure your resume highlights:
- CTA experience
- TMF handling
- GCP knowledge
- Clinical trial exposure
