Cadila Pharmaceuticals Hiring Research Associate – Pre-Clinical

Cadila Pharma Hiring Research Associate in Dholka | CRO Clinical Research Jobs

Clinical research professionals searching for CRO jobs in Gujarat now have an excellent opportunity with Cadila Pharma. The company is currently hiring Research Associates for its CRO department at Dholka, Gujarat. This full-time clinical research opportunity is ideal for candidates with experience in BA/BE studies, volunteer coordination, study documentation, and regulatory compliance within clinical research organizations and pharmaceutical research environments.

With the rapid expansion of clinical trials, bioavailability and bioequivalence studies, healthcare research operations, and regulatory-focused pharmaceutical development, demand for experienced clinical research professionals continues to grow across India. Cadila Pharma is actively expanding its CRO operations and looking for motivated candidates who can support study conduct, volunteer management, informed consent procedures, and clinical trial documentation activities.

Candidates with prior experience in clinical trial coordination, volunteer screening, healthcare compliance, study documentation, and BA/BE research operations will find this opportunity highly valuable for career advancement in the pharmaceutical and clinical research industry.

Company Overview

Cadila Pharma is one of India’s leading pharmaceutical companies with a strong presence in pharmaceutical manufacturing, clinical research, healthcare innovation, and global drug development. The company has established itself as a trusted organization within the pharmaceutical and life sciences industry through its commitment to quality, research excellence, and regulatory compliance.

The organization operates across multiple therapeutic areas and supports advanced pharmaceutical research activities including bioavailability and bioequivalence studies, clinical trials, healthcare analytics, and drug development programs.

Cadila Pharma’s CRO division plays a major role in supporting clinical research operations, volunteer management, sample handling, study documentation, and regulatory compliance processes. Employees gain exposure to GCP standards, SOP-based clinical operations, healthcare compliance systems, and regulated pharmaceutical research environments.

The company also provides employees with opportunities to build expertise in clinical research management, healthcare operations, documentation practices, and pharmaceutical regulatory systems.

Job Role & Responsibilities

Cadila Pharma is hiring candidates for the role of Research Associate under the CRO department. Selected candidates will support clinical research operations, volunteer coordination activities, study documentation, and BA/BE study execution.

This clinical research role requires candidates to possess strong documentation abilities, communication skills, regulatory understanding, and volunteer management capabilities.

Key Responsibilities

• Handle subject registration and volunteer recruitment activities
• Support volunteer screening and participant coordination processes
• Obtain informed consent according to SOP and clinical trial guidelines
• Maintain screening records and study-related documentation
• Coordinate blood and urine sample collection and transfer activities
• Ensure compliance with study protocols, SOPs, GCP guidelines, and regulatory requirements
• Facilitate study check-in and check-out activities for volunteers
• Support BA/BE study conduct activities as Study Custodian
• Coordinate with internal teams to maintain smooth clinical trial operations
• Assist in maintaining accurate healthcare and clinical research records

Preferred Technical Skills

Candidates applying for this CRO and clinical research role should have practical knowledge in:

• Clinical research operations
• BA/BE study management
• Volunteer coordination
• Informed consent procedures
• GCP compliance
• SOP documentation
• Regulatory compliance
• Healthcare documentation management
• Sample collection coordination
• Clinical trial processes
• CRO operations
• Study record maintenance

Candidates with prior exposure to pharmaceutical clinical research, healthcare compliance systems, and regulated research environments will have an added advantage.

Eligibility / Qualifications

Candidates interested in this Research Associate vacancy should meet the following eligibility criteria.

Educational Qualification

Applicants should possess a Bachelor’s or Master’s degree in Life Sciences, Pharmacy, Clinical Research, or related healthcare fields.

Eligible educational qualifications include:

B.Pharm, M.Pharm, Pharm.D, BSc, MSc, Biotechnology, Clinical Research, Biochemistry, Microbiology, Life Sciences, Biomedical Sciences, Healthcare Management, Pharmaceutical Sciences, Nursing, Medical Laboratory Sciences, or related healthcare and life science disciplines.

Experience Required

• Experience Required: 1 to 3 Years
• Prior experience in CRO operations, BA/BE studies, volunteer management, or clinical research preferred
• Knowledge of GCP guidelines, SOPs, and clinical trial documentation will be beneficial

Essential Skills

• Attention to detail
• Volunteer handling and coordination skills
• Documentation and compliance management abilities
• Team collaboration and communication skills
• Knowledge of healthcare research processes
• Organizational and multitasking capabilities
• Understanding of regulatory compliance requirements

Candidates interested in clinical research careers, CRO jobs, pharmaceutical research operations, and healthcare compliance roles are encouraged to apply.

Why Join Cadila Pharma?

Cadila Pharma provides strong career opportunities for professionals looking to grow in clinical research, CRO operations, pharmaceutical development, and healthcare compliance.

Employee Benefits

• Exposure to regulated clinical research environments
• Opportunities to work on BA/BE studies and healthcare research projects
• Experience in volunteer management and study coordination
• Career growth opportunities in CRO and pharmaceutical sectors
• Exposure to healthcare compliance and regulatory systems
• Professional learning opportunities within pharmaceutical research operations
• Collaborative and process-driven work environment

Cadila Pharma supports professional growth, healthcare innovation, and quality-focused pharmaceutical research practices.

Location & Salary

Job Location

Dholka, Gujarat

Application Process

Interested and eligible candidates can apply by sharing their updated CV with the recruitment team.

Email ID: savitri.thakor@cadilapharma.com

Frequently Asked Questions (FAQs)

1. What is the role offered by Cadila Pharma?

Cadila Pharma is hiring candidates for the position of Research Associate under the CRO department.

2. What qualifications are eligible for this CRO job?

Candidates with B.Pharm, M.Pharm, Pharm.D, BSc, MSc, Biotechnology, Clinical Research, and related life sciences qualifications can apply.

3. How much experience is required for this role?

Applicants should have 1 to 3 years of experience in clinical research, CRO operations, BA/BE studies, or healthcare research activities.

4. What is the job location for this role?

The job location for this Research Associate position is Dholka, Gujarat.

5. What skills are important for this position?

Volunteer coordination, clinical documentation, GCP compliance, healthcare research processes, and regulatory compliance skills are important for this role.

6. Does this role involve BA/BE study activities?

Yes, selected candidates will support BA/BE study conduct activities and work as Study Custodian within the CRO department.

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