Senior Clinical Research Associate – CNS/Psychiatry

Worldwide Clinical Trials

. Manage research activities at sites participating in Worldwide’s clinical research projects .

Posted 9/23/2026full-timeRemote • United StatesSenior💰 $97,000 - $193,000 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in managing clinical research activities, ensuring compliance with regulatory requirements, and effectively communicating with site personnel. Proficient in utilizing CTMS and EDC systems to support clinical studies in CNS/Neurology and Psychiatry.

Highest-signal resume keywords

Clinical Research Associate ExperienceCNS/Neurology ExperienceEDC Systems ProficiencyMicrosoft Office ProficiencyRegulatory Compliance Management

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Research ManagementStudy Start-Up ActivitiesData Collection TrainingSafety-Event ReportingStudy Maintenance Management

Soft Skills

Interpersonal CommunicationOrganizational SkillsAttention to DetailAbility to Work Independently

Tools & Technologies

CTMSEDC SystemsMicrosoft Office

Certifications & Qualifications

4-Year University DegreeNursing Degree

Industry Keywords

Clinical ResearchInformed ConsentSafety-Event ReportingMidAtlantic RegionNortheast United States

About the role

Key responsibilities & impact

Manage research activities at sites participating in Worldwide’s clinical research projects
Participate in all stages of clinical studies, including identifying potential sites
Perform study start-up activities, collect regulatory documents, and support contract and budget negotiations
Train sites to collect data properly and report potential safety-related events
Manage site activities during study maintenance
Close down research activities at sites after study completion
Conduct study initiation visits (SIVs)
Ensure compliance with informed consent, safety-event reporting, and applicable regulatory requirements while managing sites remotely

Requirements

What you’ll need

Excellent interpersonal, oral, and written communication skills in English
Superior organizational skills with attention to detail
Ability to work with little or no supervision
Proficiency in Microsoft Office, CTMS, and EDC Systems
5+ years of experience as a Clinical Research Associate
4-year university degree OR Nursing Degree
Experience in CNS/Neurology and/or Psychiatry required
Candidates must reside in the MidAtlantic or Northeast United States
Willingness to travel regionally required

Benefits

Comp & perks

Extensive support through regulatory submissions, TMF management, and in-house CRAs for projects with heavy site management needs
Regular touchpoints and coaching conversations with Line Manager
Clear career path and professional development leading to Clinical Trial Manager roles
Accessible Executive Leadership team
Competitive benefits package depending on location
Transparent compensation and pay equity