Wockhardt Limited Hiring For Clinical Research Associate / 4 days ago
Wockhardt Limited, one of India’s leading pharmaceutical and biotechnology companies, is hiring Clinical Research Associates for its Wockhardt Research Centre located in Chhatrapati Sambhajinagar, Maharashtra. Candidates with B.Pharm or M.Pharm qualifications and 2-4 years of Clinical Research experience are invited to apply.
If you are looking for Clinical Research Associate Jobs in Maharashtra, Wockhardt Jobs 2026, or Pharma Clinical Research Jobs, this is an excellent opportunity to work with an organization committed to innovation, patient safety, and regulatory excellence.
Job Highlights
| Particular | Details |
|---|---|
| Company | Wockhardt Limited |
| Position | Clinical Research Associate |
| Department | Clinical Research |
| Experience | 2-4 Years |
| Qualification | B.Pharm / M.Pharm |
| Job Location | Chhatrapati Sambhajinagar, Maharashtra |
| Employment Type | Full-Time |
| Industry | Pharmaceutical Research |
Key Responsibilities
Selected candidates will be responsible for:
- Conducting BA/BE and Clamp Studies according to Good Clinical Practice (GCP) guidelines.
- Ensuring compliance with NDCT Rules and regulatory requirements.
- Preparing Trial Master File (TMF), Study Files, Informed Consent Forms (ICF), and Case Report Forms (CRF).
- Reviewing clinical trial data and maintaining data integrity.
- Preparing study reports and submitting them to Quality Control (QC), Quality Assurance (QA), and archival teams.
- Supporting regulatory compliance throughout clinical studies.
- Maintaining proper clinical documentation and trial records.
Educational Qualification
Candidates must possess:
Experience Required
- 2 to 4 years of experience in Clinical Research
- Experience in BA/BE Studies, Clinical Trial Documentation, GCP Guidelines, and Regulatory Compliance will be preferred.
Preferred Skills
- Clinical Trial Management
- Good Clinical Practice (GCP)
- BA/BE Studies
- Clamp Studies
- Trial Master File (TMF)
- Case Report Forms (CRF)
- Informed Consent Forms (ICF)
- Data Integrity
- Regulatory Documentation
- Quality Assurance Documentation
- Report Preparation
- Strong Communication Skills
Why Join Wockhardt?
Working with Wockhardt offers professionals an opportunity to contribute to advanced pharmaceutical research while developing expertise in clinical operations.
Benefits
- Work with a reputed pharmaceutical company
- Exposure to regulated clinical research projects
- Career growth in Clinical Research
- Hands-on experience with regulatory documentation
- Collaborative research environment
- Learning opportunities with experienced professionals
- Competitive salary and employee benefits
How to Apply
Interested candidates can send their updated CV to:
