IQVIA

Clinical Research Associate – Sponsor Dedicated

IQVIA

full-time

Posted on:

Location Type: Office

Location: CaliforniaKansasUnited States

Visit company website

Explore more

AI Apply
Apply

Salary

💰 $64,000 - $189,000 per year

About the role

  • Performing site selection, initiation, monitoring and close-out visits
  • Maintaining appropriate documentation
  • Supporting the development of a subject recruitment plan
  • Establishing regular lines of communication plus administering protocol and related study training to assigned sites
  • Evaluating the quality and integrity of site practices – escalating quality issues as appropriate
  • Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution

Requirements

  • A Bachelor's degree in a health care or other scientific discipline or educational equivalent
  • Successful completion of a CRA Trainee Program or at least three months of on-site monitoring experience
  • 2 years of clinical research coordinator experience strongly preferred
  • Alternatively, an equivalent combination of education, training and experience
Benefits
  • Award winning and innovative work environment
  • Access to cutting-edge in-house technology
  • Dedicated mentoring and structured quarterly reviews on performance, promotion and bonus awards
Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills & Tools
site selectionmonitoringdocumentationsubject recruitment plan developmentprotocol administrationquality evaluationregulatory submissions trackingcase report form (CRF) completiondata query resolution
Soft Skills
communicationorganizational skills
Certifications
Bachelor's degreeCRA Trainee Program completion