Senior Clinical Research Associate – Psychiatry/Alzheimer's

Worldwide Clinical Trials

. Manage clinical research activities at investigative sites participating in Worldwide clinical studies .

Posted 10/12/2026full-timeUnited StatesSenior💰 $97,000 - $193,000 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in managing clinical research activities, including site selection, monitoring, and regulatory compliance, with a strong focus on Psychiatry and Alzheimer's clinical trials. Proven ability to collaborate with sites and study teams to ensure data quality and participant safety.

Highest-signal resume keywords

Clinical Research ManagementPsychiatry Clinical TrialsRegulatory ComplianceSite MonitoringStudy Coordination

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Trial ProcessesSite ManagementData CollectionSafety ReportingInformed ConsentStudy InitiationInterim MonitoringCloseout VisitsFull-Service MonitoringRegulatory Documentation

Soft Skills

TrainingCollaborationCommunicationProblem-SolvingInterpersonal Skills

Certifications & Qualifications

Bachelor's DegreeNursing Degree

Industry Keywords

Clinical Research AssociateInvestigative SitesStudy Start-Up ActivitiesSite Performance MonitoringEast Coast Territory

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 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 completion of study requirements
Collaborate with sites, sponsors, and global study teams

Requirements

What you’ll need

Bachelor's Degree or a Nursing Degree
5+ years as a regional, traveling Clinical Research Associate
Required experience monitoring Psychiatry or 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
Candidates must reside within the East Coast territory
Ability to travel to investigative sites approximately 8–10 days per month

Benefits

Comp & perks

Competitive benefits package depending on location
Inclusive and equitable workplace
Transparent compensation and pay equity