Torrent Pharmaceuticals is hiring Clinical Operations Executives for its Research & Development team in Ahmedabad and Gandhinagar. The role involves clinical study start-up, site management, clinical trial monitoring, vendor coordination, clinical trial supplies, and project management.
Job Details
| Details | Information |
|---|---|
| Company | Torrent Pharmaceuticals |
| Position | Clinical Operations Executive |
| Location | Ahmedabad, Gandhinagar |
| Experience | 3–8 years |
| Openings | 2 |
| Employment Type | Full Time, Permanent |
| Department | Research & Development |
| Industry | Pharmaceutical & Life Sciences |
| Qualification | M.Pharm / Pharm.D |
| Relevant Experience | CRA experience |
| Travel Requirement | Willingness to travel 20–25 days per month |
Position
Clinical Operations Executive
The Clinical Operations Executive will support clinical studies across study start-up, site management, clinical study monitoring, clinical trial supplies, vendor management, and project management.
Key Responsibilities
Study Start-Up
- Conduct site feasibility assessments.
- Perform site evaluation and selection.
- Manage site/investigator financial and study contract execution.
- Prepare Ethics Committee (EC) submission packages.
Site Management & Clinical Study Monitoring
- Support site initiation and liaisoning.
- Conduct site staff training and re-training.
- Oversee patient recruitment and retention.
- Troubleshoot site recruitment issues.
- Perform study monitoring.
- Conduct source data verification and ensure data quality.
- Support site audits.
- Manage site close-out activities.
Clinical Trial Supplies
- Manage clinical trial supplies.
Vendor Management
- Coordinate and manage vendors involved in clinical studies.
Project Management
- Track project timelines and budgets.
- Manage site and vendor invoice payments.
- Coordinate with cross-functional teams.
Eligibility and Qualifications
Education
- M.Pharm
- Pharm.D
Experience
- 3–8 years of experience
- Experience working as a Clinical Research Associate (CRA).
Other Requirement
- Willingness to travel 20–25 days per month.
Required Skills
- Regulatory understanding.
- Clinical study monitoring.
- Site management.
- Site feasibility and selection.
- Vendor coordination.
- Project tracking.
- Clinical trial supplies management.
- Source data verification and data quality management.
Application Details


