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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, including site selection, monitoring, and regulatory compliance, with a strong focus on psychiatric clinical trials. Proven ability to train site personnel and ensure data quality and participant safety throughout the study lifecycle.
Highest-signal resume keywords
Clinical Research ManagementPsychiatric Clinical Trials MonitoringRegulatory ComplianceSite ManagementTraining and Development
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Clinical Trial ProcessesSite SelectionData CollectionSafety ReportingStudy InitiationInterim MonitoringCloseout VisitsRegulatory DocumentationContract and Budget ProcessesFull-Service Monitoring
Soft Skills
CollaborationCommunicationProblem-SolvingOrganizational SkillsInterpersonal Skills
Certifications & Qualifications
Bachelor's DegreeNursing Degree
Industry Keywords
Clinical Research AssociateInvestigative SitesInformed ConsentParticipant SafetyStudy SuccessEast Coast 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 Pre-Site Selection, Study Initiation, Interim Monitoring, and Closeout Visits
- Train site personnel on protocols, data collection, and safety reporting
- Monitor site performance and provide ongoing study maintenance support
- Ensure informed consent, safety reporting, and regulatory compliance
- Partner with sites and study teams to support 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
- Required experience monitoring 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 East Coast United States territory
Benefits
Comp & perks- Competitive benefits package depending on location
- Inclusive and equitable workplace
- Transparent compensation and pay equity