Responsibilities
Identification of potential sites for studies.
Coordination with Clinical sites, vendors and internal stakeholders.
Conducting site assessment through feasibility and site qualification visit.
Provide training and guidance to sites throughout the study.
Perform monitoring visits at participating sites and review data and ensure compliance and subject safety and wellbeing.
Preparing the report, supporting the PM in drafting the plans, collection of information, adherence to study timelines
Qualification & Experience
M.Pharm, / MSc
4 years experience in related field
Computers, proficiency in word and excel, exp. Of working with clinical trial systems like ctms, edc, etc.
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