Senior Clinical Research Associate
Core
Senior Clinical Research Associate performing full-cycle site monitoring, managing trial supplies, and leading regional project activities for Phase II/III clinical studies.
Role type
Senior Clinical Research Associate (CRA)
Builds
Clinical trial data integrity and regulatory compliance for pharmaceutical studies
Domain
Clinical Research / Life Sciences
Deliverable
client delivery
Required skills
Full-cycle site monitoring, enrollment management, deviation handling, data query resolution, trial risk management, supply chain coordination, audit support, regulatory submission assistance, mentorship
Preferred skills
Feasibility assessment, study set-up, Oncology/Hematology therapeutic experience
Technologies
MS Word, Excel, PowerPoint
Responsibilities
Act as liaison between project team, sponsor, and trial sites; Perform full-cycle site visits (selection, initiation, routine, close-out); Manage investigational products and trial supplies; Oversee site feasibility and start-up; Lead country-level project calls and supervise audit activities; Mentor junior monitors
Seniority
Senior, hands-on IC with leadership responsibilities
