Phase I CRA - Early Clinical Development (Travel Required)

IQVIA

Sacramento (CA)

On-site

USD 90,000 - 175,000

Full time

14 days+

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Job summary

IQVIA is seeking a Clinical Research Associate (CRA) to join our Early Clinical Development team across West and East Coast, focusing on Phase I trials. You will monitor sites to ensure protocol compliance, regulatory adherence, and data integrity, while supporting trial execution in a dynamic environment.

Ideal candidates have a life sciences background, at least 1.5 years of on-site monitoring experience, and travel readiness to support US projects.

Qualifications

Bachelor’s degree in life sciences or health-related field, or equivalent experience.
1.5+ years of on-site monitoring experience.
Strong understanding of GCP/ICH guidelines and regulatory requirements.
Willingness and ability to travel as required by projects.

Responsibilities

Conduct site visits (selection, initiation, monitoring, close-out) per GCP/ICH guidelines.
Collaborate with site staff on recruitment strategies aligned with timelines.
Deliver protocol training to site personnel and maintain ongoing communication.
Assess site performance and escalate quality concerns as needed.
Monitor regulatory submissions, enrollment, CRFs, and data queries.
Maintain TMF/ISF documentation per regulatory standards.
Document site management activities and follow-up actions.
Collaborate with cross-functional teams to support study execution.
Support site recruitment planning and budget tracking when applicable.