Clinical Research Associate II – Metabolic

Worldwide Clinical Trials

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

Posted 11/9/2026full-timeRemote • United StatesMid-Level💰 $79,500 - $158,500 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in managing clinical research activities, including site selection, regulatory compliance, and monitoring of clinical trials, particularly in Cardiometabolic and Hypertension studies. Proven ability to train site personnel and ensure data quality and participant safety throughout the study lifecycle.

Highest-signal resume keywords

Clinical Research ManagementSite MonitoringRegulatory ComplianceCardiometabolic Trials ExperienceTraining and Support

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Trial ProcessesSite ManagementRegulatory DocumentationData CollectionSafety ReportingStudy Initiation VisitsInterim Monitoring VisitsCloseout VisitsFull-Service MonitoringBudget Processes

Soft Skills

CommunicationCollaborationProblem-SolvingTrainingSupport

Certifications & Qualifications

Bachelor's DegreeNursing Degree

Industry Keywords

Clinical Research AssociateInvestigative SitesInformed ConsentParticipant SafetyStudy SuccessTravel Requirements

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 Visits, Study Initiation Visits, Interim Monitoring Visits, and Closeout Visits
Train site personnel on protocol requirements, data collection, and safety reporting
Monitor site performance and provide ongoing support during study maintenance
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 and completion of study requirements
Travel to investigative sites approximately 8–10 days per month

Requirements

What you’ll need

Bachelor's Degree or a Nursing Degree
3+ years as a regional, traveling Clinical Research Associate
Experience monitoring Cardiometabolic and Hypertension 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 territory
Ability to support site visits and study activities across the Central / West Coast of the United States

Benefits

Comp & perks

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