Senior Clinical Research Associate – CNS
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Job Description
Senior Clinical Research Associate monitoring CNS clinical trials across Czechia for Worldwide Clinical Trials, a global contract research organization. Managing sites, compliance, data quality, and study closeout.
Responsibilities:
- 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:
- 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:
- 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
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