Clinical Research

Company Description Sun Pharma is the world’s fourth-largest specialty generic pharmaceutical company and the leading pharmaceutical company in India, providing high-quality, affordable medicines in over 100 countries. Its global operations are supported by more than 40 manufacturing facilities across 5 continents, extensive R&D centers, and a multicultural workforce representing over 50 nationalities. Sun Pharma invests significantly in research and development, with around 3,000 scientists and annual R&D spending of 6–8% of revenues, driving innovation and excellence. The organization emphasizes collective success, empowering people to grow and take charge in an environment with broad development opportunities. Through its Employee Value Proposition “Create Your Own Sunshine,” anchored on Better Every Day, Take Charge, and Thrive Together, Sun Pharma supports employees in achieving ambitious career and personal goals.
Role Description This full-time Clinical Research role at Sun Pharma is based in Ahmedabad and follows a hybrid work model, combining on-site responsibilities with some work-from-home flexibility. The role involves planning, coordinating, and executing clinical studies in line with regulatory and ethical guidelines, including drafting protocols, managing study documentation, and supporting submissions. Daily tasks include collaborating with cross-functional teams, monitoring study progress and timelines, ensuring data quality and integrity, and assisting with safety reporting and compliance activities. The role also includes reviewing scientific literature, supporting statistical analysis and clinical study reports, and contributing to continuous improvement in clinical research processes.
Qualifications

• Strong foundation in clinical research methodologies, GCP, and ICH guidelines, with the ability to apply regulatory and ethical standards in study design and conduct.
• Experience in clinical trial operations, including protocol development, site coordination, data management, and documentation for regulatory submissions.
• Ability to analyze and interpret clinical data, review scientific literature, and contribute to the preparation of reports, publications, and presentations.
• Effective communication and collaboration skills for working with cross-functional teams, investigators, and external partners in a multicultural environment.
• Proficiency with standard office and clinical research tools (e.g., EDC systems, MS Office), and strong organizational skills for managing multiple projects and timelines.
• Relevant academic background such as a degree in Pharmacy, Life Sciences, Medicine, or a related field; advanced qualifications or certifications in clinical research are an advantage.
• Demonstrated commitment to quality, attention to detail, and continuous learning; prior experience in the pharmaceutical industry or in a similar clinical research role is preferred.