Chennai, Tamil Nadu, India
Detail oriented with As a TMF (Trial Master File) Specialist, in the field of clinical research and pharmaceutical development. Oversee the Trial Master File. Also involve in managing and maintaining the Trial Master File throughout the trial's lifecycle, ensuring that all required documents are complete, accurate, and up to date. Also work closely with various stakeholders, including clinical research coordinators, investigators, regulatory authorities, and sponsors, to ensure compliance with regulatory guidelines and Good Clinical Practice (GCP) standards. Document Management with veeva vault, perform quality control to meet the required standards and guidelines. Collaborative with various stakeholders and provide training and support to the team members