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Hiring Clinical Research Associate
🏢 Sun Pharma
📍 Mumbai
🧪 Clinical Trials
📑 CRA / Site Monitoring
🎓 1–5 Years
Sun Pharma Laboratories Ltd is hiring Clinical Research Associates (CRA) for its Clinical Research Business Unit in Mumbai.
This opportunity is ideal for candidates interested in Clinical Trials, Site Monitoring, Regulatory Compliance, Clinical Operations, Pharmacovigilance, and Drug Development.
📘 Career Guide: Clinical Research Career Guide
📋 Sun Pharma CRA Recruitment 2026 – Overview
- Position: Clinical Research Associate (CRA)
- Company: Sun Pharma
- Department: Clinical Research Business Unit
- Location: Mumbai
- Employment Type: Full-Time
- Experience: 1–5 Years
- Industry: Clinical Research / Pharmaceutical Industry
- Clinical Trial Phases: Phase III & Phase IV
💰 Estimated Salary: ₹5 – ₹12 LPA
📌 Key Responsibilities
- Conduct site feasibility assessments and investigator selection
- Manage site initiation and activation activities
- Prepare Ethics Committee (EC) submission documents
- Perform site initiation, monitoring, and close-out visits
- Ensure compliance with ICH-GCP and clinical trial regulations
- Monitor patient recruitment and retention activities
- Perform Source Data Verification (SDV) and query management
- Manage Investigational Product (IP) accountability
- Support SAE and SUSAR reporting activities
- Implement CAPA activities for identified site risks
- Coordinate with CROs, Data Management, and project teams
📚 Learn Clinical Trial Basics: Clinical Trial Assistant Quiz
🎓 Eligibility Criteria
- B.Pharm / M.Pharm
- Pharm.D
- BSc / MSc Life Sciences
- Biology
- Chemistry
- Nursing
- Public Health
- PGDCR (Post Graduate Diploma in Clinical Research)
📌 Experience Required:
- 1–5 years in Clinical Research or Clinical Trials
- Experience in Phase III & IV studies preferred
💻 Required Skills
- Strong understanding of ICH-GCP guidelines
- Clinical trial monitoring expertise
- Site management and investigator coordination
- Regulatory documentation and compliance knowledge
- SAE/SUSAR reporting understanding
- Cross-functional collaboration abilities
- Communication and analytical skills
🧠 Practice Here: Clinical Research Quizzes
🎁 Why Join Sun Pharma?
- Work with India’s leading pharmaceutical company
- Exposure to global clinical trials and regulatory frameworks
- Professional growth through CRA training programs
- Opportunity to work on Phase III & Phase IV studies
- Collaborative and innovation-driven work culture
- Career advancement in Clinical Operations & Drug Development
📚 Learn More About Clinical Careers: Healthcare IT vs Clinical Healthcare
💡 Interview Tips
- Revise ICH-GCP and clinical trial phases thoroughly
- Understand CRA responsibilities and monitoring workflows
- Prepare questions on SAE/SUSAR reporting
- Practice SDV and query resolution concepts
- Revise CAPA and regulatory submission basics
- Be confident discussing clinical trial experience and projects
📊 Interview Preparation: Healthcare Interview Guide
📄 Resume Tips
- Highlight Clinical Research and CRA experience clearly
- Add GCP certifications and monitoring exposure
- Mention site management and regulatory activities
- Keep resume ATS-friendly and professional
- Include communication and documentation strengths
- Use clean formatting without spelling mistakes
📚 Career Guidance: Healthcare Career Knowledge Hub
❓ Frequently Asked Questions
- Which location is hiring? Mumbai.
- What experience is required? 1–5 years in Clinical Research.
- What trial phases are involved? Phase III & IV clinical trials.
- Which qualifications are eligible? Pharmacy, Nursing, Public Health, Life Sciences, and PGDCR candidates.
- What is the primary focus of this role? Clinical trial monitoring and site management.
🚀 Job Application Link
📌 Important Note Before You Apply:
Please make sure to read the complete job description carefully before submitting your application. Ensure your clinical research experience, GCP knowledge, and monitoring skills align with the role requirements before proceeding.
Please make sure to read the complete job description carefully before submitting your application. Ensure your clinical research experience, GCP knowledge, and monitoring skills align with the role requirements before proceeding.
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