Senior Clinical Research Associate (Sr CRA) - Client dedicated (FSP)
Core
Senior Clinical Research Associate conducting on-site and remote monitoring of clinical trial sites to ensure protocol and regulatory compliance.
Role type
Senior Clinical Research Associate (Sr CRA)
Builds
Clinical trials for pharmaceutical and biotech sponsors
Domain
Clinical Research / Life Sciences
Deliverable
client delivery
Required skills
Risk-based monitoring, root cause analysis, ICH-GCP guidelines knowledge, site feasibility assessment, contract negotiation support, audit readiness, data review (SDR/SDV/CRF), investigator management
Preferred skills
Mentoring junior CRAs, process improvement, cross-functional collaboration
Technologies
Clinical Trial Management System (CTMS)
Responsibilities
Monitor investigator sites using risk-based approach; ensure data accuracy through document review; manage site initiation and close-out; support CRO setup and regulatory licensing; mentor junior team members; prepare reports and track trial progress
Seniority
Senior, hands-on IC