Senior Clinical Research Associate – CNS
Worldwide Clinical Trials
Posted: 10/19/2026
Local Clinical Study Manager – Eastern Europe
IQVIA
Posted: 10/4/2026Senior Clinical Research Associate – CNS
Worldwide Clinical TrialsCore Competencies
Role fitCore Competencies
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Demonstrates expertise in managing clinical research activities, including site selection, regulatory compliance, and monitoring clinical trials. Proficient in training site personnel and ensuring data quality and participant safety throughout the study lifecycle.
Highest-signal resume keywords
Clinical Research ManagementSite MonitoringRegulatory ComplianceClinical Trial ProcessesTraining and Support
About the role
Key responsibilities & impact- Manage clinical research activities at investigative sites participating in Worldwide clinical studies
- Identify and assess potential research sites
- Coordinate study start-up activities, including regulatory documentation and contract and budget processes
- Conduct Pre-Site Selection Visits, Study Initiation Visits, Interim Monitoring Visits, and Closeout Visits
- Train site personnel on protocol requirements, data collection, and safety reporting
- Monitor site performance and provide ongoing support during study maintenance
- Ensure informed consent, safety reporting, and regulatory compliance
- Partner with sites and study teams to drive data quality, participant safety, and study success
- Support site closeout and completion of study requirements
Requirements
What you’ll need- Bachelor's Degree or a Nursing Degree
- 5+ years as a regional, traveling Clinical Research Associate
- Experience monitoring clinical trials
- Requires travel within the specified region; 6–8 DOS monthly
- Experience in full-service monitoring preferred
- Strong knowledge of clinical trial processes, site management, and regulatory requirements
- Candidates must reside within Czechia
- Ability to travel to investigative sites approximately 6–8 days per month
Benefits
Comp & perks- Equal employment opportunities regardless of race, color, ethnicity, ancestry, religion, national origin, gender, sex, gender identity or expression, sexual orientation, age, citizenship, marital or parental status, disability, military status, or other class protected by applicable law
ATS Keywords
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Hard Skills
Clinical ResearchSite ManagementRegulatory DocumentationData CollectionSafety ReportingMonitoring Clinical TrialsStudy InitiationCloseout VisitsFull-Service MonitoringProtocol Requirements
Soft Skills
CommunicationCollaborationProblem-SolvingOrganizational SkillsInterpersonal Skills
Certifications & Qualifications
Bachelor's DegreeNursing Degree
Industry Keywords
Clinical TrialsInvestigative SitesInformed ConsentParticipant SafetyStudy Success