Sun Pharma Clinical Research Associate Jobs 2026 offer an excellent opportunity for professionals interested in clinical trials, site monitoring, and pharmaceutical research operations. CRA - Clinical Research Associate role allows candidates to work closely with investigators, manage clinical trial sites, and ensure compliance with regulatory guidelines.
If you have experience in clinical research, site monitoring, Good Clinical Practice (GCP), and Phase III or Phase IV clinical trials, this opportunity can help you grow your career in pharmaceutical clinical operations. Candidates with a background in life sciences, pharmacy, or healthcare fields are encouraged to apply.
About Sun Pharma
Sun Pharma Laboratories Ltd is one of the largest pharmaceutical companies with a global presence in specialty generics, innovative medicines, and advanced research. The company focuses on high-quality drug development and clinical research programs aimed at improving patient care worldwide. Professionals joining the organization gain exposure to global regulatory standards, innovative clinical trials, and a collaborative work culture that supports career growth.
Sun Pharma Clinical Research Associate Job Details Overview
| Job Title | Clinical Research Associate (Clinical Trials) |
| Company Name | Sun Pharma Laboratories Ltd |
| Location | Hyderabad, India |
| Employment Type | Full Time |
| Application Deadline | Not Specified |
| Category | Latest Pharma Walk-in Interview |
Clinical Research Associate Job Responsibilities
- Perform site feasibility assessments and identify potential investigators for clinical trials.
- Negotiate study budgets with investigators and finalize investigator and site selection.
- Execute Confidentiality Disclosure Agreements (CDA) and study-related contracts.
- Prepare and submit study documents for Ethics Committee permission across multiple centers.
- Oversee investigational product dispensing, inventory management, and reconciliation.
- Ensure timely site initiation, monitoring visits, and site close-out activities with proper reports.
- Train investigators and site personnel on study protocols, procedures, and GCP principles.
- Ensure recruitment of trial participants and maintain accurate data entry and source data verification.
- Resolve data queries and maintain trial documentation as per regulatory requirements.
- Ensure timely reporting of SAEs and SUSARs in accordance with pharmacovigilance policies.
- Identify risks at clinical trial sites and implement corrective and preventive actions.
- Coordinate with CRO partners and internal teams for data management, statistical analysis, and database lock.
Required Qualifications and Skills for Clinical Research Associate
- Bachelor's or Master’s degree in a health or related field such as Biology, Chemistry, Nursing, Pharmacy, or Public Health.
- Post Graduate Diploma in Clinical Research may also be considered.
- Relevant experience of 1–5 years minimum in the field of Clinical Research.
- Knowledge of GCP practices and regulatory guidelines in clinical trials.
- Experience with Phase III and Phase IV clinical trials.
- Strong site management expertise.
- Ability to collaborate with cross-functional stakeholders.
Preferred Skills
- Experience managing multiple clinical trial sites simultaneously.
- Strong documentation and regulatory compliance knowledge.
- Excellent communication and coordination abilities.
- Analytical thinking and risk management capabilities.
Salary and Benefits
Salary for the Clinical Research Associate position will be provided as per company norms and may vary depending on experience, qualifications, and industry exposure.
How to Apply for Sun Pharma CRA
- Review the job requirements carefully.
- Prepare an updated resume highlighting your clinical research experience.
- Click the application link below to submit your details.
- Complete the online application process with accurate information.
Interview Tips for Clinical Research Associate Role
- Prepare strong knowledge of GCP guidelines and clinical trial regulations.
- Understand the full clinical trial lifecycle including site initiation, monitoring, and close-out.
- Be ready to explain experience with SAE reporting, data verification, and protocol compliance.
- Highlight experience managing investigators and coordinating with CRO partners.
Career Growth Opportunities
Professionals working as Clinical Research Associates can advance to senior roles such as:
- Senior Clinical Research Associate
- Clinical Trial Manager
- Clinical Operations Manager
- Global Clinical Project Manager
- Regulatory Affairs or Pharmacovigilance Specialist
Sun Pharma Clinical Research Associate Jobs FAQs
What qualifications are required for a Clinical Research Associate role?
Candidates must have a Bachelor’s or Master’s degree in Pharmacy, Nursing, Biology, Chemistry, Public Health, or a related healthcare field. A Postgraduate Diploma in Clinical Research may also be accepted.
How much experience is required for this job?
The position requires a minimum of 1–5 years of relevant experience in clinical research or clinical trial monitoring.
What are the key responsibilities of a Clinical Research Associate?
The CRA manages clinical trial sites, ensures protocol compliance, performs monitoring visits, supports data verification, and coordinates with investigators and research teams.
Is knowledge of GCP mandatory for this role?
Yes, strong knowledge of Good Clinical Practice guidelines and regulatory requirements for clinical trials is essential.
Conclusion
The Clinical Research Associate opportunity provides professionals with hands-on exposure to clinical trial monitoring, regulatory compliance, and investigator coordination. Candidates with experience in clinical research and strong knowledge of GCP guidelines can build a rewarding career in pharmaceutical research and clinical operations by applying for this role.


