Clinical Research Associate – Sponsor Dedicated
IQVIA
full-time
Posted on:
Location Type: Office
Location: Parsippany • Kansas, New Jersey, North Carolina • 🇺🇸 United States
Visit company websiteSalary
💰 $71,900 - $169,300 per year
Job Level
JuniorMid-Level
Tech Stack
Google Cloud Platform
About the role
- Perform monitoring and site management work to ensure sites conduct studies as required
- Conduct site monitoring visits in accordance with GCP and regulatory requirements
- Manage the progress of assigned studies by tracking regulatory submissions and approvals
- Collaborate and liaise with study team members for project execution support
Requirements
- Bachelor's Degree in scientific discipline or health care preferred
- At least 1 year of on-site monitoring experience
- Good knowledge of applicable clinical research regulatory requirements (i.e., GCP and ICH guidelines)
- Computer skills including proficiency in Microsoft Word, Excel, and PowerPoint
- Effective time and financial management skills
Benefits
- Health insurance
- Retirement plans
- Paid time off
- Professional development
- Bonuses
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard skills
site monitoringregulatory submissionsGCPICH guidelines
Soft skills
time managementfinancial management