Posted:8 hours ago|
Platform:
Work from Office
Full Time
Coordinate day-to-day activities of clinical trials from initiation to close-out.
Recruit, screen, and enroll eligible participants as per study protocol.Schedule and conduct study visits, ensuring adherence to study timelines.Maintain accurate and timely documentation including case report forms (CRFs), informed consent forms (ICFs), and other trial-related documents.Liaise between the sponsor, investigators, ethics committees, and internal teams.Ensure compliance with ICH-GCP guidelines and regulatory requirements.Monitor patient safety and report adverse events (AEs/SAEs) promptly.Support audits and inspections by regulatory authorities or sponsors.Manage study supplies, including investigational products and lab kits.Assist in training new clinical staff and support site readiness for future trials.
Certification in clinical research (ACRP, SOCRA, etc.) is an added advantage.
Experience with Electronic Data Capture (EDC) systems.
Familiarity with regulatory submissions and ethics approvals.
Medi Pharma Konnect
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