Clinical Research Associate
Core
Conduct onsite monitoring visits, manage clinical study startups, and verify source documents for various therapeutic indications.
Role type
Clinical Research Associate
Builds
Clinical studies across multiple therapeutic areas
Domain
Life Sciences / Clinical Research
Required skills
Onsite monitoring, Source document verification, CRF review, Query resolution, Site management, Feasibility research, Regulatory document preparation, Audit/inspection support
Preferred skills
MS Office proficiency, Planning and multitasking, Team collaboration, Problem-solving
Technologies
MS Office
Responsibilities
Conduct and report onsite monitoring visits, Perform study startup activities, Support regulatory team in preparing submission documents, Participate in audits and inspections
Seniority
Junior, hands-on IC
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