Looking for the latest Clinical Trial Assistant jobs in Noida? Curadev has announced an exciting opportunity for the position of Clinical Trial Assistant (CTA) in Noida / New Delhi. Candidates with an interest in clinical operations, TMF management, clinical documentation, and GCP compliance can apply for this clinical research job opportunity.
This Clinical Trial Assistant vacancy is ideal for freshers and candidates with experience in clinical research, life sciences, pharmacy, biotechnology, or related healthcare domains who want to build a career in clinical trials and regulatory operations.
Job Details
| Particulars | Details |
|---|---|
| Job Role | Clinical Trial Assistant (CTA) |
| Company | Curadev |
| Location | Noida / New Delhi |
| Industry | Clinical Research / Biotechnology |
| Employment Type | Full-Time |
| Department | Clinical Operations |
| Experience | Freshers & Experienced |
| Mode of Application |
Key Responsibilities of Clinical Trial Assistant
Clinical Trial Operations Support
- Provide operational support to clinical study teams daily.
- Assist in study start-up, maintenance, and close-out activities.
- Track study timelines, milestones, and deliverables.
- Maintain study dashboards, trackers, and status reports.
- Coordinate internal and external clinical trial meetings.
Trial Master File (TMF/eTMF) Management
- Maintain and upload essential documents in TMF/eTMF systems.
- Ensure TMF quality, completeness, and inspection readiness.
- Track regulatory and site essential document collection.
- Support periodic TMF reconciliation activities.
Site & CRA Coordination
- Support CRAs in site management and documentation activities.
- Track site activation, monitoring visits, and close-out status.
- Coordinate investigator communication and document collection.
- Assist in study material preparation and distribution.
Regulatory & Compliance Activities
- Ensure compliance with ICH-GCP guidelines, SOPs, and local regulations.
- Track ethics committee and IRB approvals.
- Support audit and inspection readiness activities.
- Assist in safety reporting documentation and filing.
Vendor & Logistics Coordination
- Coordinate with CROs, laboratories, and imaging vendors.
- Support logistics and shipment tracking for study materials.
- Assist with vendor documentation and contract tracking.
Clinical Systems & Data Management
- Maintain study information in CTMS and eTMF systems.
- Support investigator databases and contact lists.
- Track study metrics and data queries.
Administrative Support
- Prepare meeting agendas, MOMs, and follow-up action items.
- Support travel coordination and meeting logistics.
Required Qualifications
Candidates applying for this Clinical Trial Assistant job in Noida should preferably have:
- B.Pharm, M.Pharm, Pharm.D, BSc, MSc, Biotechnology, Life Sciences, or related qualification
- Basic understanding of clinical research processes
- Knowledge of ICH-GCP guidelines and clinical documentation
- Familiarity with TMF, eTMF, CTMS, or regulatory systems is preferred
- Good communication and coordination skills
- Strong documentation and organizational abilities
Why Join Curadev?
Working with Curadev offers candidates exposure to:
- Clinical trial operations
- TMF/eTMF management
- Regulatory compliance activities
- Clinical research documentation
- Cross-functional collaboration with study teams and vendors
- Career growth opportunities in clinical research and biotech sectors