Assessing the eligibility of the volunteers for participation in the study
Training of SOP's of clinical staff
Supervise the administration of investigational products, ICF Process and all study activities from check-in to check out as per the applicable protocol and GCP guidelines.
Management of Medical emergencies during studies
Management of post-study adverse event
Preparation of SOP.
Reviewing documents generated during the study.
Assist the CI/PI in the medical aspect of the study
Preparation of adverse event data for compilation in the final study report.
Medical examination during screening.
Any other responsibility assigned by the Head Clinical
Employement Category:
Employement Type: Full timeIndustry: Medical / HealthcareRole Category: DoctorFunctional Area: Not ApplicableRole/Responsibilies: Mbbs Doctor