Clinical Trial Job at Sun Pharma for Freshers | Apply
Discover an exciting clinical trial job opportunity at Sun Pharma Laboratories Ltd, based at the Sun House Corporate Office in Mumbai. This role is ideal for freshers and early-stage professionals exploring Sun Pharma careers or looking to enter the expanding field of clinical research jobs in Mumbai. Join a company that empowers you to grow, innovate, and contribute meaningfully to global healthcare.
Clinical Trial Job Details:
- Job Title: Clinical Trial Assistant
- Business Unit: Clinical Research
- Location: Sun House – Corporate Office, Mumbai
About the Company
Sun Pharma Laboratories Ltd is a global pharmaceutical leader known for its innovation, customer focus, and commitment to healthcare excellence. As one of the top destinations for sun pharma careers, the company encourages individuals to “Create your own sunshine” through continuous personal and professional development. With a culture built on collaboration, ownership, and growth, Sun Pharma supports employees in becoming better every day while contributing to high-impact clinical research initiatives.
Educational Qualification:
Bachelor’s or Master’s degree in a health-related field or Public Health
Experience:
Relevant experience of 0-2 years minimum in the field of Clinical Research.
Job Description:
This clinical trial job offers the unique opportunity to support clinical studies within the Clinical Research business unit. The Clinical Trial Assistant plays an essential role in documentation, regulatory support, and coordination. It is a strong fit for those pursuing clinical research jobs in Mumbai and seeking to contribute to compliant, efficient, and meaningful clinical trial operations.
Key Responsibilities for This Clinical Trial Job:
Documentation and Administrative Support:
- Assist in the maintenance of study documentation, including protocols, informed consent forms, case report forms, and study reports.
- Help organize and maintain electronic and paper-based study files, ensuring accuracy and completeness.
- Provide administrative support, including scheduling meetings, preparing meeting minutes, and coordinating travel arrangements as needed.
Regulatory Compliance Support:
- Assist in the preparation and submission of regulatory documents to ethics committees and regulatory authorities.
- Support the maintenance of regulatory compliance by ensuring adherence to Good Clinical Practice (GCP) guidelines and local regulations.
Site Coordination & Communication:
- Assist in tracking invoice generation and payment process for all sites.
- Perform vendor code generation and vendor tracking.
