Clinical Research Associate

IQVIA

Clinical Research Associate managing clinical sites to ensure compliance in clinical trials at IQVIA. Collaborating with site staff and supporting study execution and data integrity.

Posted 5/27/2026full-timeDurham • New York, North Carolina, Texas • 🇺🇸 United StatesJuniorMid-Level💰 $71,900 - $169,300 per yearWebsite

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Conduct all types of site visits—selection, initiation, monitoring, and close-out in alignment with contracted scope of work, GCP, and ICH guidelines
Collaborate with site staff to implement and track subject recruitment strategies
Deliver protocol and study-specific training to site personnel
Assess site performance and adherence to the protocol
Monitor study progress by tracking regulatory submissions and subject enrollment
Ensure that essential documents are collected and maintained in accordance with regulatory standards
Document site management activities, visit outcomes, and follow-up actions
Work closely with cross-functional project teams to support study execution

Requirements

What you’ll need

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

Comp & perks

Health insurance
Retirement plans
Paid time off

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills & Tools

site monitoringsubject recruitment strategiesprotocol trainingregulatory submissions trackingdocument managementperformance assessmentstudy execution support

Soft Skills

collaborationcommunicationorganizational skillsattention to detail