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Senior Clinical Research Associate – Psychiatry
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, training personnel, and supporting study success within the CNS and psychiatric domains.
Highest-signal resume keywords
Clinical Research ManagementSite MonitoringRegulatory ComplianceCNS Clinical Trials ExperienceTraining and Development
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
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Hard Skills
Clinical Trial ProcessesSite ManagementRegulatory DocumentationData CollectionSafety ReportingStudy Start-Up ActivitiesFull-Service MonitoringInformed ConsentSite Closeout ActivitiesBudget Processes
Soft Skills
CollaborationCommunicationProblem-SolvingLeadership
Certifications & Qualifications
Bachelor's DegreeNursing Degree
Industry Keywords
Clinical Research AssociateInvestigative SitesPSSVsSIVsIMVsCOVsParticipant SafetyStudy MaintenanceCentral United States
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 support study maintenance activities
- 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
Requirements
What you’ll need- Bachelor's Degree or a Nursing Degree
- 5+ years as a regional, traveling Clinical Research Associate
- Experience monitoring CNS and psychiatric 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 Central of the United States territory
Benefits
Comp & perks- Competitive benefits package depending on location
- Transparent compensation and pay equity