Support the setup, initiation, and monitoring of clinical trials.
Assist in preparing essential documents, trial master files (TMF), and regulatory submissions.
Help coordinate communication between sponsors, sites, and vendors.
Participate in site selection and qualification visits under supervision.
Ensure data accuracy, integrity, and compliance with study protocols.
Support the review of informed consent forms and other trial-related documents.
Assist in tracking study progress and maintaining study databases.
Participate in team meetings and training related to GCP and company SOPs.
Report and document adverse events as per protocol and regulatory guidelines.
Ensure confidentiality and ethical conduct in all research activities.
Job Types: Full-time, Permanent, Fresher
Pay: ?24,217.15 - ?43,780.99 per month
Benefits:
Health insurance
Paid sick time
Provident Fund
Work Location: In person
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