
Prajwal Tandale
@prajwaltandale
I support compliant clinical trial documentation, TMF activities, and study coordination.
What I'm looking for
At G7, I support clinical trial activities and study documentation in line with protocols, SOPs, and Good Clinical Practice requirements.
I assist with preparing, reviewing, filing, and maintaining study records, including TMF/eTMF documentation. I contribute to organized, complete, traceable documentation and timely follow-up of study-related activities.
With a B.Pharm background and ICH-GCP training, I bring knowledge of clinical research processes, informed consent, pharmacology, and trial compliance. I'm seeking a Clinical Trial Assistant role where I can help deliver efficient, compliant trial execution.
Experience
Work history, roles, and key accomplishments
Trainee Clinical Trial Associate
G7
Supported clinical trial activities and study documentation in compliance with protocols, SOPs, and GCP. Assisted with TMF/eTMF organization, document review, and study coordination.
Education
Degrees, certifications, and relevant coursework
Varadaraja Institute of Pharmaceutical Education and Research
Bachelor of Pharmacy, Pharmacy
Pursued Bachelor of Pharmacy, gaining knowledge in pharmaceutical sciences and clinical research.
Tech stack
Software and tools used professionally
Availability
Location
Authorized to work in
Salary expectations
Job categories
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