Clinical Trial Associate(Sun pharma)

Roles and Responsibilities

YOUR TASKS AND RESPONSIBILITIES:

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 tracking of vendors.

Educational Qualification

Minimum qualification requirement is to have a Bachelor's or Master’s degree in a health related field, such as Biology, Chemistry, Nursing, Pharmacy, or Public Health and/or Post-graduate Diploma in Clinical Research.

Experience

Relevant experience of 0-2 years minimum in the field of Clinical Research.