Senior Clinical Research Associate (Sr. CRA) – Oncology | Sponsor-Aligned
Location: Overland Park, Kansas (Field-Based)
Job Type: Full-Time
Job ID: R1482206
IQVIA is seeking a highly experienced Senior Clinical Research Associate (Sr. CRA) to support sponsor-aligned oncology programs, with a primary focus on Phase 1 oncology trials. This position plays a key role in ensuring high-quality site monitoring, regulatory compliance, and efficient study execution across assigned clinical trial sites.
Job Overview
The Senior CRA will be responsible for monitoring and managing clinical research sites to ensure adherence to study protocols, Good Clinical Practice (GCP), International Council for Harmonisation (ICH) guidelines, and sponsor-specific requirements. This role offers the opportunity to support innovative oncology research impacting patient care and treatment outcomes worldwide.
Key Responsibilities
Clinical Site Monitoring
Conduct site selection, initiation, routine monitoring, and close-out visits in accordance with GCP, ICH, and study-specific guidelines.
Ensure accurate, consistent, and timely data collection across all clinical trial sites.
Recruitment & Site Support
Develop and track site-level subject recruitment strategies aligned with project timelines.
Provide protocol, safety, and study-specific training to site staff while maintaining continuous communication.
Quality & Compliance Oversight
Assess site performance, protocol adherence, and regulatory compliance.
Identify, document, and escalate quality issues when necessary.
Study Progress Management
Oversee regulatory document submissions, patient recruitment status, CRF completion, data query resolution, and other essential study activities.
Support clinical trial start-up activities as required.
Documentation & Reporting
Maintain complete and accurate filing of study documents in the Trial Master File (TMF) and Investigator Site File (ISF).
Prepare monitoring visit reports, follow-up letters, and site correspondence.
Mentorship & Collaboration
Mentor junior clinical staff through co-monitoring and training activities.
Work closely with cross-functional study teams to ensure seamless project execution.
Required Qualifications
Education
Bachelor’s degree required.
A degree in a scientific or healthcare discipline is strongly preferred.
Experience (Mandatory)
Minimum 3+ years of on-site oncology monitoring experience strongly preferred.
Candidates with at least 1.5+ years of oncology monitoring experience may be considered.
Phase 1 oncology (early-phase) monitoring experience is required.
Technical Skills
Strong working knowledge of GCP, ICH, and relevant clinical research regulations.
Advanced understanding of Phase 1 oncology protocols.
Proficiency in Microsoft Word, Excel, PowerPoint, and digital tools.
Professional Skills
Strong written and verbal communication abilities.
Excellent organizational, analytical, and problem-solving skills.
Effective time management and ability to prioritize workload across multiple sites.
Ability to build and maintain professional site relationships and collaborate with internal teams.
Why Join IQVIA?
This role provides the opportunity to contribute to cutting-edge Phase 1 oncology research, work directly with leading sponsor teams, and make a direct impact in advancing cancer therapies. IQVIA offers a collaborative environment, global exposure, and career growth opportunities within clinical operations.
Compensation
Annual base pay range: USD 57,500 – USD 226,800.
Final compensation depends on experience, qualifications, location, and work schedule. Additional incentives, bonuses, and comprehensive benefits may be offered.
Equal Opportunity Statement
IQVIA is an equal opportunity employer and welcomes applicants regardless of race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.
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