IQVIA

Clinical Research Associate

IQVIA

full-time

Posted on:

Location Type: Office

Location: Durham • New York, North Carolina, Texas • 🇺🇸 United States

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Salary

💰 $71,900 - $169,300 per year

Job Level

JuniorMid-Level

Tech Stack

Google Cloud Platform

About the role

  • Conduct all types of site visits—selection, initiation, monitoring, and close-out in alignment with the contracted scope of work, Good Clinical Practice (GCP), and ICH guidelines.
  • Collaborate with site staff to implement and track subject recruitment strategies that align with project timelines and enrollment goals.
  • Deliver protocol and study-specific training to site personnel and maintain consistent communication to manage expectations and resolve issues.
  • Assess site performance and adherence to the protocol, escalating quality concerns as needed to ensure compliance and data integrity.
  • Monitor study progress by tracking regulatory submissions, subject enrollment, case report form (CRF) completion, and resolution of data queries.
  • Ensure that essential documents are collected and maintained in both the Trial Master File (TMF) and the Investigator Site File (ISF) in accordance with regulatory standards.
  • Document site management activities, visit outcomes, and follow-up actions through detailed reports and correspondence.
  • Work closely with cross-functional project teams to support study execution and ensure alignment with project goals.

Requirements

  • Bachelor’s degree in life sciences or health-related field (or equivalent experience)
  • Requires at least 1 year of on-site monitoring experience
  • Strong understanding of GCP, ICH guidelines, and regulatory requirements
  • Ability to travel as required by the project
Benefits
  • Health insurance
  • Competitive salary
  • 401(k) matching
  • Professional development opportunities

Applicant Tracking System Keywords

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

Hard skills
site monitoringsubject recruitment strategiesprotocol trainingdata integrityregulatory submissionscase report form (CRF) completionTrial Master File (TMF)Investigator Site File (ISF)documentationreport writing
Soft skills
communicationcollaborationproblem-solvingorganizational skillsattention to detailtime managementexpectation managementquality assessmentcross-functional teamworkissue resolution