Senior Clinical Research Associate – CNS
Lifelancer
Posted: 10/19/2026
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
LifelancerCore Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in managing clinical research activities, ensuring regulatory compliance, and monitoring clinical trials. Proficient in site management, training personnel, and driving data quality and participant safety.
Highest-signal resume keywords
Clinical Research ManagementMonitoring Clinical TrialsRegulatory ComplianceSite ManagementTraining Site Personnel
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 processes, and safety reporting expectations
- 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- Must reside within Czechia
- Bachelor's Degree or a Nursing Degree
- 5+ years as a regional, traveling Clinical Research Associate
- Required experience monitoring clinical trials
- Willingness and ability to travel within the specified region, approximately 6–8 days per month
- Experience in full-service monitoring preferred
- Strong knowledge of clinical trial processes, site management, and regulatory requirements
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
- Home-based/remote work arrangement
- Global team collaboration
- Supportive, cohesive teams and accessible leadership
- Diverse and inclusive work environment
- Employee opportunity to influence clinical study success and support high-quality study delivery
ATS Keywords
✓ Tailor your resumeApplicant Tracking System Keywords
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Hard Skills
Clinical Trial ProcessesData Collection ProcessesSafety ReportingStudy Start-Up ActivitiesSite Performance MonitoringInformed ConsentFull-Service MonitoringInterim MonitoringCloseout VisitsPre-Site Selection Visits
Soft Skills
CollaborationCommunicationProblem-SolvingSupportTraining
Certifications & Qualifications
Bachelor's DegreeNursing Degree
Industry Keywords
Clinical Research AssociateInvestigative SitesRegulatory DocumentationContract ProcessesBudget ProcessesParticipant SafetyStudy SuccessCzechia