Responsible for coordinating and performing (if applicable) the collection, distribution and storage/ archival of data/ study material/ study supply generated (for assigned studies) during clinical research trials.

Responsible to ensure that the assigned trials stay on track with applicable regulations, GCP, Protocol and Tech Observer/ Sponsor SOP’s.

Maintain databases of patient information; collect information for grant proposals and write correspondence.

Maintain Investigator database and search current potential Investigators for upcoming trials.
Enter data from forms and documents into databases as required for assigned studies.
Provide assistance to operational team by organizing files, projects, data and keeping it up to date for assigned studies.





Maintain Trial Master File (TMF) in coordination with APM/PM for assigned studies.
Assist CRA for the maintenance of the Site Master File ( SMF)

Assist with routine in-house data verification and quality control, ensuring data integrity and consistency with prescribed study protocol for assigned studies.

Use Standard Operating Procedures (SOPs) concepts, practices in a time sensitive manner.
Assist CRA in investigator meeting preparation, liaison, presentations, and follow up for assigned studies.

Assist CRA in tracking the Investigator site

📌 Senior Clinical Trial Associate (Surat)
🏢 Tech Observer
📍 Surat