Clinical Research Associate Jobs: Explore Sunpharma Careers & Apply Now
Clinical Research Associate Jobs- Sun Pharma Laboratories Ltd is inviting passionate clinical research professionals to join its growing Clinical Research team as a Clinical Research Associate (CRA) in Nagpur. This position offers an excellent opportunity to work on impactful clinical studies that advance patient safety, drug efficacy, and regulatory excellence. The role is ideal for individuals with a background in life sciences or pharmacy who aspire to contribute meaningfully to the world of clinical trials and evidence-based medicine.
Clinical Research Associate Jobs—Details:
- Job Title: Clinical Research Associate
- Location: Nagpur
About the Company:
Sun Pharma Laboratories Ltd is one of the world’s leading pharmaceutical companies, committed to delivering high-quality, affordable healthcare globally. With a presence in over 100 countries, Sun Pharma drives innovation across therapeutic areas, including cardiology, psychiatry, neurology, gastroenterology, and oncology. The company’s culture is built around its core values—growth, integrity, and collaboration—empowering employees to “Create Your Own Sunshine.” At Sun Pharma, professionals are encouraged to grow continuously, take charge of their careers, and thrive in a supportive and purpose-driven community.
Clinical Research Associate Jobs—Role:
The Clinical Research Associate (CRA) plays a pivotal role in ensuring the effective execution, monitoring, and documentation of clinical trials in compliance with Good Clinical Practice (GCP) and regulatory requirements. The role involves close collaboration with investigators, site personnel, and internal stakeholders to maintain data integrity and ensure the successful completion of studies. The CRA is responsible for ensuring high-quality trial conduct, ethical compliance, and timely reporting to support Sun Pharma’s commitment to advancing safe and effective healthcare solutions.
Key Responsibilities
- Conduct site feasibility assessments, identify potential investigators, and negotiate study budgets.
- Oversee preparation and submission of study documents for Ethics Committee (EC) approvals across sites.
- Manage investigational product (IP) dispensing, inventory control, and reconciliation documentation.
- Conduct site initiation, routine monitoring, and close-out visits, ensuring timely completion of reports.
- Train investigators and site staff on study protocols, procedures, and GCP principles.
- Monitor patient recruitment progress and ensure accuracy of data entry, source data verification, and query resolution.
- Oversee reporting of SAEs (Serious Adverse Events) and SUSARs in accordance with regulatory timelines and pharmacovigilance policies.
- Identify site-related risks, perform root cause analyses, and implement Corrective and Preventive Actions (CAPA).
- Coordinate with internal or CRO partners for data management, statistical analysis, and database lock activities.
Qualifications & Experience
- Bachelor’s or Master’s degree in a health-related field (Biology, Chemistry, Nursing, Pharmacy, or Public Health)
OR Postgraduate Diploma in Clinical Research. - 1–5 years of relevant experience in clinical research, preferably in Phase III and Phase IV trials.
- In-depth understanding of GCP principles, clinical trial regulations, and site management.
Explore SunPharma Careers & Join Now:
At Sun Pharma, success is built on continuous growth and shared achievement. Employees are empowered to lead with confidence, collaborate across teams, and contribute to innovations that improve global health outcomes. The company provides robust benefits, learning opportunities, and a culture that encourages both personal and professional development.
