If you’re a life sciences professional with hands-on experience in clinical trials, this is a strong opportunity to grow your career with Sun Pharmaceutical Industries Ltd.. Known for its global presence and innovation-driven approach, Sun Pharma offers a platform where professionals can contribute to impactful research while advancing their careers.
🧪 About the Role
The Clinical Research Associate (CRA) role sits within the Medical Affairs & Clinical Research division. This mid-level position is ideal for professionals who are ready to take ownership of clinical study execution and work in a fast-paced environment.
📍 Location: Mumbai
💼 Experience: 3–5 years
🎓 Qualification: Bachelor’s or Master’s degree in Life Sciences or related field
🔍 Key Responsibilities
As a CRA, you will be responsible for ensuring clinical studies are conducted efficiently, ethically, and in compliance with regulations.
📌 Clinical Trial Management
- Manage CRO-led and in-house clinical studies
- Support feasibility assessments and site selection
- Oversee execution of interventional and observational studies
🏥 Site & Investigator Coordination
- Identify investigators and trial sites
- Coordinate study initiation and execution
- Ensure site readiness and compliance
📄 Regulatory & Documentation Work
- Prepare submissions for Ethics Committees and Drug Controller General of India (DCGI)
- Maintain essential trial documentation
- Ensure compliance with New Drugs and Clinical Trial Rules, 2019
⚠️ Safety Reporting
- Report SAEs and SUSARs within timelines
- Coordinate safety communication across stakeholders
🤝 Vendor & Stakeholder Management
- Manage CRO partnerships
- Collaborate with Regulatory, QA, and Medical Affairs teams
- Oversee budgets, contracts, and vendor performance
📚 Skills & Expertise Required
To succeed in this role, candidates should bring both technical expertise and strong coordination skills:
✔️ In-depth knowledge of ICH-GCP guidelines
✔️ Experience in remote and risk-based monitoring
✔️ Exposure to audits and regulatory inspections
✔️ Familiarity with ICMR guidelines (2017) and Drugs & Cosmetics Act
✔️ Ability to work in cross-functional teams
✔️ Strong communication and stakeholder management skills
📝 How to Apply
Interested candidates can apply directly through the official job listing using the link below:
Make sure your resume is updated and highlights your clinical research experience, monitoring activities, and regulatory knowledge to increase your chances of selection.
🚀 Why Consider This Role?
Clinical research is one of the most impactful career paths in healthcare. This role offers:
✨ Exposure to multi-site and global clinical trials
📈 Strong career growth in pharma and biotech
🌍 Collaboration with international teams
🧠 Continuous learning in regulatory and clinical domains
🧑⚕️ Who Should Apply?
This opportunity is best suited for:
- CRAs with 3–5 years of experience
- Professionals from CRO, pharma, or biotech sectors
- Candidates skilled in monitoring, audits, and submissions
- Individuals passionate about clinical research and patient safety
💡 Career Tip
To stand out, ensure your resume highlights:
- Experience across clinical trial phases (I–IV)
- Site monitoring visits and study management
- Audit and inspection exposure
- Regulatory submissions and pharmacovigilance work
📢 Final Thoughts
This CRA role in Mumbai is a solid career move for professionals looking to advance in clinical research. With growing demand for skilled CRAs in India, opportunities like this offer both stability and long-term growth. If you meet the criteria, this could be your next big step 🚀
