Senior Clinical Research Associate – CNS, Psychiatry
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Worldwide Clinical TrialsPosted 10/19/2026full-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 facilitating effective communication among site teams. Proficient in coordinating study start-up and maintenance while delivering high-quality clinical trial outcomes.
Highest-signal resume keywords
Clinical Research Associate ExperiencePsychiatry ExperienceStudy Initiation Visits (SIVs)Microsoft Office ProficiencyCTMS and EDC Systems Proficiency
About the role
Key responsibilities & impact- Manage research activities at investigative sites participating in Worldwide’s clinical research projects
- Support sites throughout the full study lifecycle, from site identification and start-up through study maintenance and close-out
- Coordinate study start-up activities, including collecting required regulatory documentation and supporting contract and budget negotiations
- Conduct Study Initiation Visits (SIVs) and train sites on accurate data collection and safety-event reporting
- Manage ongoing site activities, primarily remotely, while maintaining effective communication and oversight
- Ensure sites comply with informed consent requirements, safety reporting expectations, and applicable regulatory requirements
- Partner with site teams to support high-quality study conduct and successful clinical trial delivery
- Collaborate with investigative sites, sponsors, and global study teams
- Travel to investigative sites approximately 8-10 days per month
Requirements
What you’ll need- A four-year university degree or Nursing Degree
- 5+ years of experience as a Clinical Research Associate
- Experience in Psychiatry required
- Experience in full-service monitoring PREFERRED
- Excellent interpersonal, organizational, and communication skills, with strong attention to detail
- Ability to work effectively with little or no supervision
- Proficiency in Microsoft Office, CTMS, and EDC systems
- Proficiency in English, including strong oral and written communication skills
- Candidates must reside within the Southeast territory
- Ability to travel to investigative sites approximately 8-10 days per month
Benefits
Comp & perks- Regular coaching conversations
- Professional development support
- Career path that can lead to Clinical Trial Manager opportunities
- Competitive benefits package depending on location
- Inclusive and equitable workplace
ATS Keywords
✓ Tailor your resumeApplicant Tracking System Keywords
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Hard Skills
Clinical Research ManagementRegulatory Documentation CollectionData Collection TrainingSafety-Event ReportingSite Compliance MonitoringContract Negotiation SupportBudget Negotiation SupportStudy Lifecycle ManagementFull-Service MonitoringAttention to Detail
Soft Skills
Interpersonal SkillsOrganizational SkillsCommunication SkillsAbility to Work IndependentlyEffective Communication
Certifications & Qualifications
Four-Year University DegreeNursing Degree
Industry Keywords
Clinical TrialsInvestigative SitesInformed ConsentSafety ReportingSoutheast Territory