Metropolis Healthcare is recruiting for the Clinical Trial Associate position in Mumbai, Maharashtra. The role involves clinical trial project setup and management, study documentation, specimen tracking, report release, and coordination with sponsors and investigator sites.
Candidates with a B.Sc. degree in Clinical Pathology, Microbiology, Genetics, or Biotechnology and 1β3 years of experience can explore this opportunity.
Job Details
| Particulars | Details |
|---|---|
| Company | Metropolis Healthcare |
| Job Title | Clinical Trial Associate |
| Location | Mumbai, Maharashtra |
| Experience | 1β3 years |
| Vacancies | 3 |
| Employment Type | Full-time, Permanent |
| Qualification | B.Sc. in Clinical Pathology, Microbiology, Genetics, or Biotechnology |
| Industry | Medical Services / Diagnostics |
| Travel Required | No |
Position: Clinical Trial Associate
The Clinical Trial Associate will coordinate clinical trial project setup activities after a study is awarded to Metropolis Healthcare. The role includes preparing study-specific documentation, coordinating specimen logistics, monitoring inventory, and ensuring timely report release.
---Advertisement---
Key Responsibilities
- Initiate and manage clinical trial project setup activities.
- Customize TRFs, LIM, test profiles, dummy reports, kit letters, and client code requests.
- Coordinate logistics to ensure timely specimen receipt and complete project setup before FPFV.
- Release study reports within committed turnaround times (TATs).
- Resolve queries from sponsors and investigator sites.
- Ensure studies follow applicable SOPs and sponsor guidelines.
- Document problem data and problem specimens in coordination with investigators.
- Maintain updated specimen status and kit inventory trackers.
- Support the Quality Assurance (QA) team during study and sponsor audits.
- Perform quality checks on study-related documents.
Eligibility and Qualifications
Candidates should have:
- Education: B.Sc. in Clinical Pathology, Microbiology, Genetics, or Biotechnology.
- Experience: 1β3 years.
- Experience in clinical trial project setup and management.
- Strong documentation skills and knowledge of clinical trial operations.
Required Skills
- Clinical research and clinical trial management
- Clinical trial project setup
- Study documentation and quality checks
- Specimen tracking and inventory management
- Report release and turnaround time management
- Sponsor and investigator query resolution
- SOP compliance and audit support
- Clinical operations coordination
---Advertisement---
