Freshers Clinical Trial Job at Sun Pharma
Are you searching for a rewarding Clinical Trial Job in India’s leading pharmaceutical sector? Here’s an exciting opportunity for life science graduates to join Sun Pharma as a Clinical Trial Associate. This role offers hands-on exposure to clinical research, regulatory processes, and real-world drug development, making it an ideal launchpad for freshers and early-career professionals in life sciences.
About Sun Pharma
Sun Pharma is one of India’s largest and most trusted pharmaceutical companies, known for its global presence and innovation in healthcare. With a strong focus on research and development, Sun Pharma provides excellent career opportunities and fosters growth for professionals seeking a Clinical Trial Job in the pharma industry.
Job Details:
- Job Title: Clinical Trial Associate
- Company: Sun Pharma Laboratories Ltd
- Location: Mumbai
- Office: Sun House – Corporate Office
- Business Unit: Medical Affairs & Clinical Research
About the Role
Sun Pharma Laboratories Ltd is seeking a Clinical Trial Associate to support its Medical Affairs & Clinical Research team. The role involves assisting in clinical trial documentation, regulatory processes, and site coordination while ensuring compliance with industry standards.
The organization fosters a growth-oriented and collaborative environment where employees are encouraged to take initiative, continuously improve, and contribute to shared success.
Key Responsibilities
- Documentation and Administrative Support
- Assists in maintaining study documentation such as protocols, informed consent forms, case report forms, and study reports.
- Organizes and maintains both electronic and paper-based study files, ensuring accuracy and completeness.
- Provides administrative support, including scheduling meetings, preparing minutes, and coordinating travel arrangements when required.
- Regulatory Compliance Support
- Supports preparation and submission of regulatory documents to ethics committees and regulatory authorities.
- Ensures adherence to Good Clinical Practice (GCP) guidelines and applicable local regulations.
- Site Coordination & Communication
- Assists in tracking invoice generation and payment processes for clinical sites.
- Supports vendor code generation and maintains vendor tracking systems.
Qualifications
- Education
- Bachelor’s or Master’s degree in a health-related field, such as Biology, or a Postgraduate Diploma in Clinical Research
- Experience
- 0–2 years of relevant experience in clinical research.
