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Senior Clinical Research Associate – CNS, Psychiatry
Worldwide Clinical Trials. Manage research activities at investigative sites participating in Worldwide clinical research projects .
Posted 10/14/2026full-timeRemote • North Carolina • United StatesSenior💰 $97,000 - $193,000 per yearWebsite
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in managing clinical research activities, ensuring compliance with regulatory requirements, and effectively collaborating with investigative sites and study teams. Proficient in data collection, safety event reporting, and full-service monitoring within the Psychiatry domain.
Highest-signal resume keywords
Clinical Research Associate ExperiencePsychiatry ExpertiseRegulatory Compliance ManagementMicrosoft Office ProficiencyCTMS and EDC Systems Knowledge
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 Research ManagementData CollectionSafety Event ReportingStudy Start-Up CoordinationFull-Service Monitoring
Soft Skills
Interpersonal CommunicationOrganizational SkillsAttention to DetailWritten Communication
Tools & Technologies
CTMSEDC SystemsMicrosoft Office
Industry Keywords
Clinical ResearchInvestigative SitesRegulatory DocumentsInformed ConsentStudy Lifecycle Management
About the role
Key responsibilities & impact- Manage research activities at investigative sites participating in Worldwide clinical research projects
- Support sites throughout the clinical study lifecycle, from identification and start-up through maintenance and closeout
- Coordinate study start-up activities, including collecting appropriate regulatory documents and supporting contract and budget negotiations
- Conduct study initiation visits and train sites on accurate data collection and safety event reporting
- Monitor site activities and help ensure compliance with informed consent, safety reporting, and applicable regulatory requirements
- Partner with sites and study teams to address site management needs and support successful study delivery
- Travel to investigative sites approximately 8–10 days per month
- Collaborate with sites, sponsors, and global study teams
Requirements
What you’ll need- Bachelor’s degree from a four-year university or a Nursing Degree
- 5+ years of experience as a Clinical Research Associate
- Experience in Psychiatry
- Excellent interpersonal, oral, and written communication skills, including proficiency in English
- Strong organizational skills with excellent attention to detail and the ability to work with little or no supervision
- Proficiency in Microsoft Office, CTMS, and EDC systems
- Residence on the East Coast
- Willingness to travel regionally
- Experience in full-service monitoring PREFERRED
Benefits
Comp & perks- Competitive benefits package depending on location
- Regular coaching and development conversations
- Clear career path that can lead to Clinical Trial Manager opportunities
- Inclusive and equitable workplace
- Transparent compensation and pay equity