Who can apply for this Clinical Research job?

Candidates with B.Pharm, M.Pharm, Life Sciences, and Clinical Research qualifications can apply.

What experience is required for this role?

Applicants should have 1-3 years of experience in CRO operations or clinical research.

What is the salary range for this role?

The estimated salary range for this role is ₹3.2 LPA – ₹5.5 LPA.

How can candidates apply for this job?

Candidates can send their updated CV to savitri.thakor@cadilapharma.com.

Is this Advarra job suitable for freshers?

Yes, this role is suitable for freshers and candidates with up to 1 year of experience.

What systems are used in this role?

Candidates will work on CTMS, EDC platforms, CRF development, and clinical research workflows.

What is the salary for Research Associate I at Advarra?

The estimated salary ranges from ₹3.2 LPA to ₹5.5 LPA depending on skills and experience.

What qualifications are required for this role?

Candidates should have a degree in Pharmacy, Life Sciences, Biotechnology, Nursing, or related fields.

Cadila Pharmaceuticals Hiring Research Associate in CRO Department | Clinical Research Jobs in Gujarat 2026

Cadila Pharmaceuticals Hiring Research Associate in the CRO Department at Dholka

(Cadila Pharmaceuticals Hiring Research Associate)

Introduction

The clinical research industry in India continues to grow rapidly in 2026, creating excellent opportunities for pharmacy and life sciences professionals. Cadila Pharmaceuticals has announced a new opening for the position of Research Associate in its CRO Department located at Dholka, Gujarat. This opportunity is highly suitable for candidates who want to build a long-term career in Clinical Research, BA/BE studies, volunteer coordination, and regulatory documentation.

Candidates with experience in Good Clinical Practice (GCP), SOP compliance, study coordination, and clinical trial operations are encouraged to apply for this latest Cadila Pharma job opening. Professionals searching for Clinical Research jobs in Gujarat, CRO jobs for pharmacy graduates, and BA/BE study opportunities can benefit significantly from this role.

Author: Pharmaduniya Editorial Team

About Cadila Pharmaceuticals

Cadila Pharmaceuticals is one of India’s leading privately held pharmaceutical companies with a strong presence in domestic and international healthcare markets. Established in 1951, the company is headquartered in Ahmedabad, Gujarat, India.

Cadila Pharma operates across multiple therapeutic segments, including oncology, cardiology, respiratory, gastroenterology, and infectious diseases. The company has advanced research facilities, manufacturing plants, and clinical research operations supporting global pharmaceutical innovation.

With thousands of employees and operations across various countries, Cadila Pharmaceuticals is known for its focus on research-driven healthcare solutions, regulatory compliance, and quality pharmaceutical manufacturing. The organization also plays an important role in CRO operations, BA/BE studies, and clinical development activities in India.

Company Headquarters: Ahmedabad, Gujarat, India
Founded: 1951
Industry: Pharmaceutical & Clinical Research
Employee Strength: 10,000+ Employees Worldwide

Job Overview Summary

Cadila Pharmaceuticals is hiring Research Associates for its CRO Department in Dholka, Gujarat. The role mainly focuses on clinical trial coordination, volunteer handling, subject registration, BA/BE study support, and maintaining study documentation according to regulatory standards.

The selected candidates will work closely with clinical research teams, study coordinators, and operational departments to ensure smooth execution of BA/BE studies and compliance with SOPs, GCP guidelines, and clinical research regulations.

This role provides excellent exposure to CRO operations, clinical trial compliance, volunteer management, and regulatory documentation, making it a valuable career opportunity for pharmacy and life sciences professionals.

Vacancy Details

Particulars	Details
Job Title	Research Associate
Department	CRO (Clinical Research Organization)
Company	Cadila Pharmaceuticals
Location	Dholka, Gujarat
Experience Required	1–3 Years
Qualification	Bachelor’s/Master’s in Life Sciences, Pharmacy, Clinical Research
Employment Type	Full-Time
Industry	Pharmaceutical & Clinical Research
Salary Estimate	₹3.2 LPA – ₹5.5 LPA
Application Mode	Email Application

Research Associate Job Responsibilities Explained

Volunteer Recruitment & Coordination

The Research Associate will support volunteer registration, screening, and coordination activities during BA/BE studies. Proper communication with volunteers and maintaining accurate records are important responsibilities under this role.

Study Documentation Management

Candidates will maintain clinical trial records, informed consent documents, screening records, and study files according to SOP and GCP requirements. Accurate documentation is one of the most critical parts of clinical research operations.

Clinical Trial Compliance

The selected professional must ensure compliance with protocols, regulatory guidelines, SOPs, and Good Clinical Practice (GCP) standards during all study activities.

Sample Collection Coordination

The role also involves coordinating blood and urine sample collection, handling sample transfer activities, and ensuring proper study logistics management during clinical trial execution.

Study Operations Support

Research Associates will assist with check-in/check-out procedures, volunteer management, and BA/BE study operations while working as Study Custodians for assigned projects.

Eligibility Criteria

Educational Qualification

Candidates applying for this Clinical Research job should possess:

Bachelor’s Degree in Life Sciences
Master’s Degree in Life Sciences
B.Pharm
M.Pharm
Clinical Research Qualification
Related healthcare or science disciplines

Experience Required

1–3 years of experience in:
- CRO operations
- Clinical research
- BA/BE studies
- Clinical trial coordination

Preferred Knowledge

Good Clinical Practice (GCP)
SOP compliance
Volunteer handling
Regulatory documentation
Clinical trial processes

Skills Required

Cadila Pharmaceuticals is looking for candidates with strong operational and clinical research skills. Important skills required for this role include:

Clinical trial coordination
Volunteer management abilities
Strong documentation practices
Regulatory compliance understanding
Communication and interpersonal skills
Attention to detail
Team collaboration
Study record maintenance
BA/BE operational knowledge
Clinical research workflow understanding

Candidates with good organizational skills and the ability to work in regulated environments will have an advantage during the selection process.

Salary Estimate

Based on current pharmaceutical and CRO industry standards in India, the estimated salary for the Research Associate role at Cadila Pharmaceuticals may range between:

₹3.2 LPA – ₹5.5 LPA

Actual salary may vary depending on:

Candidate experience
BA/BE study exposure
Clinical research knowledge
Interview performance
Technical skills

Additional benefits may include:

Professional training
Clinical research exposure
Career development opportunities
Regulatory compliance experience

Interview Details

Selection Process

The selection process may include:

CV Shortlisting
HR Screening Round
Technical Interview
Final Discussion

Interview Topics

Candidates may be assessed on:

GCP Guidelines
SOP compliance
Clinical trial basics
BA/BE study process
Volunteer handling
Documentation practices
Regulatory compliance
Communication skills

Required Documents

Candidates applying for the Cadila Pharmaceuticals Research Associate role should keep the following documents ready:

Updated Resume/CV
Educational Certificates
Experience Certificates
Identity Proof
Passport-size Photograph
Clinical Research Internship Documents (if available)
Salary Slips (for experienced candidates)

Why Join Cadila Pharmaceuticals?

Working at Cadila Pharmaceuticals provides strong exposure to clinical research operations and regulated CRO environments. Employees gain practical experience in:

BA/BE studies
Volunteer coordination
Clinical documentation
Regulatory compliance
Study management
SOP implementation
Cross-functional clinical operations

The company offers a professional work environment with opportunities for long-term career growth in the clinical research and pharmaceutical industry.

How to Apply

Interested and eligible candidates can send their updated CV to:

📩 Email: savitri.thakor@cadilapharma.com

Subject Line:
Application for Research Associate – CRO Department

Candidates are advised to apply as early as possible since openings may close once suitable candidates are shortlisted.

Frequently Asked Questions (FAQs)

Q1. What is the job role offered by Cadila Pharmaceuticals?

Cadila Pharmaceuticals is hiring for the position of Research Associate in the CRO Department.

Q2. What qualifications are required for this Clinical Research job?

Candidates with B.Pharm, M.Pharm, Life Sciences, or Clinical Research qualifications can apply.

Q3. What is the required experience for this role?

Applicants should have 1–3 years of clinical research or CRO experience.

Q4. What is the job location?

The job location is Dholka, Gujarat.

Q5. Is the BA/BE study experience important for this role?

Yes, knowledge of BA/BE studies and volunteer coordination is preferred.

Q6. What is the estimated salary for this position?

The expected salary range is approximately ₹3.2 LPA – ₹5.5 LPA.

Q7. How can candidates apply for this role?

Candidates can apply by sending their updated CV to savitri.thakor@cadilapharma.com.

Final Conclusion

Cadila Pharmaceuticals offers an excellent opportunity for pharmacy and life sciences professionals looking to strengthen their careers in clinical research and CRO operations. The Research Associate role at Dholka provides valuable exposure to BA/BE studies, volunteer management, clinical documentation, and regulatory compliance activities.

Candidates interested in Clinical Research jobs in Gujarat, CRO career opportunities, and BA/BE operational roles should consider applying for this opening. With exposure to regulated environments and practical clinical trial operations, this opportunity can help candidates build a strong foundation for long-term career growth in the pharmaceutical and clinical research industry.

Disclaimer

Note: Pharma Duniya does not charge any money for job information. Candidates are advised to verify details from the official company website.

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