Senior Clinical Research Associate – FSP
Parexel
full-time
Posted on:
Location Type: Remote
Location: Remote • 🇺🇸 United States
Visit company websiteJob Level
Senior
About the role
- Responsible for the site management, site monitoring and close-out of assigned clinical trials investigator sites
- Manage investigator site relationships to ensure effective delivery of clinical trials (e.g. enrollment, database release)
- Ensure proper conduct of clinical trials in accordance with the Study Monitoring Plan (SMP)
- Work in partnership with the Site Care Partner (SCP) to ensure quality of site delivery
- Conduct onsite, remote/electronic monitoring as needed for study site initiation, routine monitoring and study site closure activities
Requirements
- Minimum 3 years relevant experience in clinical research site monitoring (preferably 2 years in Oncology)
- Preferred therapeutic experience in Oncology, Vaccines, Internal Medicine or Infectious Diseases
- Must be fluent in English and in the native language(s) of the country they will work in
- Ability to travel 60-80%
- Valid driver’s license and passport required
Benefits
- Health insurance
- Retirement plans
- Paid time off
- Flexible work arrangements
- Professional development
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard skills
clinical trials managementsite monitoringstudy site initiationroutine monitoringstudy site closure activitiesdata managementenrollment strategies
Soft skills
relationship managementcommunicationcollaborationproblem-solvingattention to detail