Apotex is inviting applications for the position of Clinical Research Associate (CRA) at its Bengaluru location. This is an excellent opportunity for experienced B.Pharm and M.Pharm graduates who have expertise in Clinical Operations, Bioequivalence Studies, Good Clinical Practice (GCP), Good Laboratory Practice (GLP), and clinical documentation.
If you are looking for Clinical Research Associate jobs in Bangalore, Apotex careers, or Bioequivalence Clinical Research jobs, this opportunity offers exposure to end-to-end clinical study execution in a globally recognized pharmaceutical organization.
Job Details
| Particular | Details |
|---|---|
| Position | Clinical Research Associate |
| Company | Apotex |
| Location | Bengaluru, Karnataka |
| Department | Research & Development |
| Employment Type | Full-Time |
| Industry | Pharmaceutical & Life Sciences |
| Experience | Minimum 5 Years in Clinical Operations |
| Qualification | B.Pharm / M.Pharm |
Key Responsibilities
As a Clinical Research Associate at Apotex, you will:
- Execute Bioequivalence and Clinical studies according to approved protocols.
- Ensure compliance with SOPs, GCP, GLP, and regulatory guidelines.
- Coordinate protocol training and study check-in activities.
- Prepare study documentation including TMF, CRFs, raw data, and clinical reports.
- Review study data for accuracy and protocol compliance.
- Perform dosing supervision, sample collection, and subject monitoring.
- Coordinate study sample transfer and subject safety follow-up.
- Generate and upload study forms using Nuleap.
- Prepare protocol status reports and clinical summaries.
- Manage study archival activities.
- Collaborate with investigators, study coordinators, and cross-functional teams.
Eligibility Criteria
Candidates should possess:
- B.Pharm or M.Pharm
- Minimum 5 years of Clinical Operations experience
- Experience in Bioequivalence Studies
- Strong knowledge of:
- Good Clinical Practice (GCP)
- Good Laboratory Practice (GLP)
- Clinical Documentation
- Trial Management File (TMF)
- Case Report Forms (CRFs)
- Excellent communication and coordination skills.
- Ability to work in a regulated clinical research environment.
Preferred Skills
- Clinical Research
- Bioequivalence Studies
- Clinical Operations
- GCP Compliance
- GLP Compliance
- Clinical Documentation
- TMF Management
- CRF Preparation
- Protocol Training
- Regulatory Compliance
Why Join Apotex?
Apotex offers professionals the opportunity to work in a globally recognized pharmaceutical company with exposure to regulated clinical research operations.
Benefits include:
- Global clinical research exposure
- Career growth in Clinical Operations
- Hands-on Bioequivalence study experience
- Collaborative work environment
- Learning opportunities with regulatory compliance standards
- Stable full-time employment
How to Apply
