Clinical Research jobs in United States
Explore 408 matching jobs.
Senior Clinical Research Associate – Psychiatry
Worldwide Clinical Trials
Posted: 10/20/2026Clinical Research Associate – Sponsor Dedicated
IQVIA
Posted: 10/20/2026Clinical Research Nurse – Home Visits
WEP Clinical
Posted: 10/20/2026Clinical Research Nurse – Home Visits, PRN
WEP Clinical
Posted: 10/20/2026Clinical Research Nurse – Home Visits
WEP Clinical
Posted: 10/20/2026Clinical Research Nurse – Home Visits
WEP Clinical
Posted: 10/20/2026Clinical Research Nurse, Home Visits
WEP Clinical
Posted: 10/20/2026Associate Principal Scientist, Clinical Research
MSD
Posted: 10/20/2026Google Cloud Platform
Biostatistician II
Thermo Fisher Scientific
Posted: 10/20/2026D
Senior Biostatistician
DefinedTalent
Posted: 10/20/2026Clinical Research Regulatory Specialist
Alcanza Clinical Research
Posted: 10/20/2026Google Cloud Platform
Senior Clinical Research Associate – CNS, Psychiatry
Worldwide Clinical Trials
Posted: 10/19/2026Senior Clinical Research Associate
ICON plc
Posted: 10/19/2026Clinical Research Nurse II
Emory University
Posted: 10/19/2026Clinical Research Nurse II
Emory University
Posted: 10/19/2026Clinical Research Associate, U.S. Expert Network
Alcedis - a HUMA company
Posted: 10/19/2026Google Cloud Platform
Senior Clinical Trial Manager
Stoke Therapeutics
Posted: 10/19/2026Senior Clinical Data Manager – Contract
BioCryst Pharmaceuticals, Inc.
Posted: 10/17/2026Assistant Manager, Clinical Research – Neurology
WashU IT
Posted: 10/17/2026Research Systems Analyst – Clinical Research Unit
WVU Online
Posted: 10/17/2026Google Cloud Platform

Senior Clinical Research Associate – Psychiatry
Worldwide Clinical TrialsCore 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 monitoring CNS and Alzheimer's studies.
Highest-signal resume keywords
Clinical Research ManagementRegulatory ComplianceCNS Clinical Trials MonitoringSite ManagementTraining and Development
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 complete 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 Alzheimer's 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
- Must reside in the Central of the United States territory
Benefits
Comp & perks- Competitive benefits package depending on location
- Transparent compensation and pay equity
ATS Keywords
✓ Tailor your resumeApplicant Tracking System Keywords
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Hard Skills
Clinical Trial ProcessesSite Performance MonitoringRegulatory DocumentationData CollectionSafety ReportingStudy Start-Up ActivitiesFull-Service MonitoringInformed Consent ProceduresBudget ManagementContract Processes
Soft Skills
CollaborationCommunicationProblem-SolvingLeadership
Certifications & Qualifications
Bachelor's DegreeNursing Degree
Industry Keywords
Clinical Research AssociateInvestigative SitesAlzheimer's TrialsParticipant SafetyStudy Closeout Activities