- Screening of volunteers.
- Review of laboratory reports, ECGs and X-ray reports.
- Preparation of selected list of volunteers in screening.
- Obtaining written consent form the volunteers for a study.
- Performing clinical examination and inclusion / exclusion criteria of volunteers during study conduct.
- Monitoring of subjects during study conduct and providing necessary care.
- Supervision of dose administration of subjects during the course of study.
- Management of adverse events during the study and providing support to PI/CI./li>
- Review of post-study laboratory reports.
- Marinating sufficient medical / clinical supplies in the ICU and providing necessary training to study staff.
- Review of literature and provide necessary support to PI for ensuring the safety of subjects.
- Supervision of ICU and ambulance.
- Providing necessary training to staff for ensuring the subject's safety.
- Quality compliance in performing the activities.
📌 Clinical Research Physician (India)
🏢 Advity Research
📍 India
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