Senior Clinical Research Associate
Core
Frontline communication with project stakeholders to ensure timelines, targets, and standards of clinical research projects across various therapeutic indications, focusing on subjects' rights, safety, well-being, and data quality compliance.
Role type
Senior Clinical Research Associate (Freelance/Contractor)
Builds
Clinical research study activities and data compliance for therapeutic indications
Domain
Clinical Research / Life Sciences
Deliverable
client delivery
Required skills
On-site monitoring, CRF review, source document verification, query resolution, site communication and management, study activity supervision, quality control and compliance monitoring
Preferred skills
Oncology and Gastroenterology study experience, MS Office (Intermediate to Advanced)
Technologies
MS Office
Responsibilities
Conducting and reporting onsite monitoring visits, performing CRF reviews and source document verification, resolving queries, managing site communication and schedules, acting as a point of contact for support services and vendors, supporting quality control and compliance reports review
Seniority
Senior, hands-on IC