Job Description

The Sub-Investigator assists the Principal Investigator (PI) in the day-to-day conduct of clinical trials. The primary role is to ensure participant safety, strictly adhere to study protocols, and manage accurate data collection, all while complying with Good Clinical Practice (GCP) and regulatory requirements.

• Participant Care & Safety: Perform study-related physical examinations, monitor for Adverse Events (AEs) and Serious Adverse Events (SAEs), and provide medical management as needed.
• Protocol Compliance: Ensure all study procedures are followed according to the approved protocol.
• Informed Consent: Review and obtain informed consent from participants per Standard Operating Procedures (SOPs).
• Documentation: Review laboratory results, patient history, and maintain accurate source documentation.
• Study Procedures: Administer study medication, perform phlebotomy, and collect specimens as required.
• Team Collaboration: Work with Study Coordinators to ensure the study is conducted smoothly.

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