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Senior Clinical Research Associate – CNS, Rare Disease
Worldwide Clinical Trials. Manage clinical research activities at investigative sites participating in Worldwide clinical studies .
Core 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 driving data quality in clinical trials. Proficient in site management, monitoring CNS and Rare Disease studies, and training site personnel on protocol requirements.
Highest-signal resume keywords
Clinical Research ManagementCNS Clinical Trials MonitoringRegulatory ComplianceSite ManagementTraining and Support
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
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Hard Skills
Clinical Trial ProcessesSite Performance MonitoringRegulatory DocumentationContract and Budget ProcessesData CollectionSafety ReportingStudy Start-Up ActivitiesStudy Closeout ActivitiesInformed ConsentFull-Service Monitoring
Soft Skills
CollaborationCommunicationProblem-SolvingSupport
Certifications & Qualifications
Bachelor's DegreeNursing Degree
Industry Keywords
Clinical Research AssociateInvestigative SitesRare DiseaseCNSStudy SuccessParticipant Safety
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 PSSVs, SIVs, IMVs, and COVs
- 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 activities and completion of study requirements
- Collaborate with sites, sponsors, and global study teams
Requirements
What you’ll need- Bachelor's Degree or a Nursing Degree
- 5+ years as a regional, traveling Clinical Research Associate
- Required experience monitoring CNS and Rare Disease clinical trials
- Requires travel within the specified region; 8–10 DOS monthly
- Experience in full-service monitoring preferred
- Strong knowledge of clinical trial processes, site management, and regulatory requirements
- Candidates must reside within the Midwest territory
- Willingness to travel to investigative sites approximately 8–10 days per month
Benefits
Comp & perks- Competitive benefits package depending on location
- Inclusive and equitable workplace
- Growth and career development opportunities
- Collaborative and inclusive work environment