Senior Clinical Research Associate
CTI Clinical Trial and Consulting Services
full-time
Posted on:
Location Type: Remote
Location: Kentucky • United States
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Job Level
About the role
- Responsible for project activities associated with monitoring functions of phase I through phase IV clinical research studies
- Conduct site visits and complete site visit deliverables with quality and within timelines
- Assist with study start-up activities, including feasibility, pre-study activities, and site selection
- Participate in investigator, client, and project team meetings
- Manage ISF and TMF for all assigned study sites in accordance with SOPs
Requirements
- At least 1 year of clinical trial monitoring experience or equivalent experience
- Bachelor's Degree or higher in an allied health field
- Previous experience in conducting clinical research studies
- Demonstrated successful performance in a CRA position with a minimum of 1 year of on-site monitoring experience preferred
Benefits
- Health benefits
- Vacation packages
- Hybrid work-from-home opportunities
- Paid parental leave
- Ongoing education and training through tuition reimbursement
- Structured mentoring program and leadership courses
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
clinical trial monitoringsite selectionfeasibility assessmentstudy start-up activitiesISF managementTMF managementSOP compliance
Soft Skills
communicationteam collaborationorganizational skillstime management
Certifications
Bachelor's Degree in allied health field