0 - 2 years
0 Lacs
Posted:1 day ago|
Platform:
On-site
Full Time
Assist in planning, initiation, monitoring, and completion of clinical trials.
Conduct site qualification, initiation, routine monitoring, and close-out visits.
Ensure all trial activities are conducted according to protocol, SOPs, GCP, and applicable regulatory guidelines.
Verify that clinical data is accurate, complete, and verifiable from source documents.
Maintain essential documents and track trial progress in the Trial Master File (TMF).
Support communication between sponsors, investigators, and site staff.
Identify and resolve issues that arise during study conduct.
Ensure subject safety and proper reporting of adverse events (AEs/SAEs).
Prepare visit reports and follow-up letters as per timelines.
Participate in investigator meetings and training sessions.
CLARIWELLGLOBAL SERVICES LLP
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