דרושים אמינולאב בע"מ

End-to-End Trial Lifecycle: Drive operational planning, study execution, and timely delivery of global clinical trials (feasibility, site selection, SIV, monitoring, and close-out).

CRO Vendor Management: Lead selection processes (RFPs, bid defense) and oversee day-to-day CRO/vendor performance, KPIs, and deliverables.

Study Execution Site Oversight: Manage site-facing activities, enrollment tracking, compliance, and build strong relationships with investigators.

data Quality TMF: Ensure data integrity, lead risk management/mitigation planning, and maintain completeness of the Trial Master File (TMF) through to database lock.

Cross-Functional Collaboration: Represent the sponsor in internal/external meetings, collaborating with Regulatory, Safety, CMC, and Biometrics while adhering to ICH-GCP.