Junior Clinical Research Associate – Transition Opportunity for ACRAs & Junior CRAs
Core
Transitioning Clinical Research Coordinators or junior CRAs into a Clinical Research Associate role to perform clinical monitoring and site management.
Role type
Junior Clinical Research Associate (monitoring)
Builds
Clinical trials across various therapeutic areas and sponsors
Domain
Clinical Research / Life Sciences
Required skills
Source data review (SDR) and verification (SDV), visit report writing, protocol and regulatory compliance knowledge, ICH-GCP guidelines, root cause analysis, site relationship management, Microsoft Office proficiency, extensive travel management
Preferred skills
Experience with sponsor-driven trials, mentorship readiness
Technologies
Microsoft Office, clinical trial software
Responsibilities
Conduct on-site and remote site visits to assess protocol and regulatory compliance, maintain accurate study documentation, identify and address site issues, ensure audit readiness, collaborate with cross-functional teams
Seniority
Junior, early-career IC