Work from Office
Full Time
Role & responsibilities To work as a study physician. Assessing the eligibility of the volunteers for participating in the study. Training of SOPs of Clinical Staff. Supervise Administration of investigational product, ICF process and all study activities from check in to check out as per applicable protocol and GCP guidelines. Management of medical emergencies during studies. Management of post study adverse event. Reveiweing of documents generated during study. Assist the CI/PI in medical aspect of the study. Preferred candidate profile Immediate to 1month joinees preferable
Lupin
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