Contract Clinical Research Associate
Core
Conduct onsite monitoring visits, perform CRF review and source document verification, and manage site communication for clinical studies across various therapeutic indications.
Role type
Contract Clinical Research Associate
Builds
Clinical studies data integrity and regulatory submission readiness
Domain
Clinical Research / Life Sciences
Deliverable
client delivery
Required skills
Independent monitoring, CRF review, source document verification, query resolution, site management, feasibility research, regulatory document preparation
Preferred skills
Latvian language knowledge, MS Office proficiency
Technologies
MS Office
Responsibilities
Conduct and report onsite monitoring visits, Perform CRF review and source document verification, Resolve queries, Manage site communication, Support regulatory team in document preparation
Seniority
Individual Contributor, Contract/Freelance