Senior Clinical Research Associate, Oncology

IQVIA

Clinical Research Associate responsible for monitoring oncology clinical trial sites at IQVIA. Ensuring compliance with protocols and regulations while contributing to groundbreaking cancer research.

Posted 6/12/2026full-timeOverland Park • California, Kansas • 🇺🇸 United StatesSenior💰 $71,900 - $189,000 per yearWebsite

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Conduct selection, initiation, monitoring, and close-out visits in line with GCP and ICH guidelines.
Collaborate with sites to develop and track recruitment plans, ensuring project needs are met.
Provide protocol and study training to sites, maintaining regular communication to manage expectations and address issues.
Assess site practices for protocol adherence and regulatory compliance, escalating quality issues as needed.
Oversee regulatory submissions, recruitment, enrollment, CRF completion, and data query resolution.
Ensure all site documents are filed in the Trial Master File (TMF) and Investigator’s Site File (ISF) per GCP/ICH and local regulations.
Generate visit reports, follow-up letters, and other necessary documentation.
Mentor clinical staff through co-monitoring and training visits.
Work closely with study team members to support project execution.

Requirements

What you’ll need

BS degree required; a degree in a scientific discipline or healthcare is preferred.
3+ years of on site oncology monitoring experience strongly preferred.
1.5+ years of oncology monitoring experience can be considered.
Phase 1 oncology experience is required.
Proficient in GCP and ICH guidelines.
Strong therapeutic and protocol knowledge in Phase 1 oncology trials.
Excellent computer skills, including Microsoft Office and mobile devices.

Benefits

Comp & perks

Health insurance
Retirement plans
Paid time off
Flexible work arrangements
Professional development opportunities

ATS Keywords

✓ Tailor your resume

Applicant Tracking System Keywords

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

Hard Skills & Tools

oncology monitoringGCP guidelinesICH guidelinesprotocol adherenceregulatory compliancedata query resolutionTrial Master File (TMF)Investigator’s Site File (ISF)recruitment plansPhase 1 oncology trials

Soft Skills

collaborationcommunicationmentoringproblem-solvingproject execution