Provide leadership and direction to clinical site management team members from study start through to closure
Serve as Site Management’s primary point of contact and representative for clinical monitoring and site activities within the project, including, but not limited to Primary Sponsor Contact
Manage monitoring deliverables to achieve the study budget and identify out-of-scope activities
Requirements
Bachelor’s Degree or a Nursing Degree required
2+ years’ experience as a Clinical Trial Manager, Clinical Operations Leader, Lead CRA, or equivalent role
3+ years’ experience as a Clinical Research Associate
Extensive Cardiovascular experience is required
Willingness to travel up to 30%
Benefits
Flexible working hours
Professional development opportunities
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.