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Nashik
Overseeing the smooth running of clinical trials.
Collecting, coding, and analyzing data obtained from research.
Managing research budgets.
Informing participants about study objectives.
Administering questionnaires.
Monitoring research participants to ensure adherence to study rules.
Adhering to research regulatory standards.
Adhering to ethical standards.
Maintaining detailed records of studies as per FDA guidelines, including things such as drug dispensation.
Liaising with laboratories regarding findings.
Participating in subject recruitment efforts.
Ensuring that the necessary supplies and equipment for a study are in stock and in working order.
Engaging with subjects and understanding their concerns.
Experience | 0 - 1 Years |
Salary | 2 Lac To 2 Lac 25 Thousand P.A. |
Industry | Pharma / R&D / Biotech |
Qualification | BAMS, B.Pharma, B.Sc, M.Sc |
Key Skills | Trainee Clinical Research Coordinator |
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