Cadila Pharmaceuticals has announced a new job opening for the position of Research Associate in the CRO Department at Dholka, Gujarat. Candidates with 1-3 years of experience in clinical research, BA/BE studies, volunteer coordination, and study documentation are encouraged to apply.
This latest Clinical Research job in Gujarat is ideal for Life Sciences, Pharmacy, and Clinical Research graduates looking to build a career in CRO operations and BA/BE studies. The company is seeking detail-oriented professionals with knowledge of GCP guidelines, SOP compliance, and subject management.
Job Overview
| Job Details | Information |
|---|---|
| Job Title | Research Associate |
| Department | CRO (Clinical Research Organization) |
| Company | Cadila Pharmaceuticals |
| Location | Dholka |
| Experience Required | 1-3 Years |
| Qualification | Bachelor’s/Master’s in Life Sciences, Pharmacy, Clinical Research |
| Job Type | Full-Time |
| Salary Range | ₹3.2 LPA – ₹5.5 LPA (Estimated) |
| Application Mode | Email Application |
Research Associate Job Responsibilities
Candidates selected for the Research Associate role at Cadila Pharma will be responsible for managing various CRO and BA/BE study activities, including:
- Subject registration and volunteer recruitment
- Volunteer screening and coordination activities
- Obtaining informed consent according to SOP guidelines
- Maintaining screening documentation and study records
- Coordinating blood and urine sample collection and transfer
- Ensuring compliance with protocols, SOPs, GCP, and regulatory standards
- Managing study check-in and check-out procedures
- Supporting BA/BE study conduct as Study Custodian
This Clinical Research Associate-style role requires strong documentation skills, volunteer coordination abilities, and adherence to clinical trial compliance standards.
Eligibility Criteria
Applicants interested in this Clinical Research job in Gujarat must meet the following qualifications:
Educational Qualification
- Bachelor’s or Master’s degree in:
- Life Sciences
- Pharmacy
- Clinical Research
- Related healthcare or science disciplines
Experience
- 1 to 3 years of relevant CRO or clinical research experience
Preferred Knowledge
- Good Clinical Practice (GCP)
- SOP compliance
- Clinical trial processes
- BA/BE study operations
Required Skills
Cadila Pharma is looking for candidates with:
- Strong attention to detail
- Volunteer handling and coordination skills
- Documentation and compliance management expertise
- Effective communication skills
- Team collaboration abilities
Why Join Cadila Pharma?
Working with Cadila Pharmaceuticals offers professionals exposure to advanced CRO operations and regulated clinical research environments. Employees gain hands-on experience in:
- BA/BE study execution
- Regulatory documentation
- Volunteer management
- Clinical operations compliance
- Cross-functional CRO coordination
This opportunity can significantly strengthen a candidate’s clinical research career profile.
How to Apply
Interested candidates can send their updated CV to:
📩 savitri.thakor@cadilapharma.com
Candidates should mention “Application for Research Associate – CRO Department” in the email subject line for faster processing.