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Senior Clinical Research Associate
Worldwide Clinical Trials. Manage clinical research activities at investigative sites participating in Worldwide clinical studies .
Posted 11/5/2026full-timeRemote • Michigan • 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, including site selection, regulatory compliance, and study monitoring. Proficient in training site personnel and ensuring data quality and participant safety throughout the clinical trial process.
Highest-signal resume keywords
Clinical Research ManagementSite MonitoringRegulatory ComplianceClinical Trial ProcessesTraining and Development
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 ActivitiesSite SelectionRegulatory DocumentationBudget ProcessesData CollectionSafety ReportingStudy InitiationInterim MonitoringCloseout VisitsFull-Service Monitoring
Soft Skills
CollaborationCommunicationProblem-Solving
Certifications & Qualifications
Bachelor's DegreeNursing Degree
Industry Keywords
Clinical TrialsInvestigative SitesInformed ConsentParticipant SafetyStudy Success
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 provide ongoing study maintenance support
- 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
- Travel to investigative sites approximately 8–10 days per month
Requirements
What you’ll need- Bachelor's Degree or a Nursing Degree
- 5+ years as a regional, traveling Clinical Research Associate
- 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
- Equal employment opportunities