Clinical Research Coordinator, On-Site, Kansas City MO
IQVIA · Kansas City, MO, United States of America · Global
Clinical Research
–
Not yet analysed
Demand78
Career growth70
Healthcare fit72
Remote potential10
5-year outlook
Entry-level CRC pay is typically modest for a healthcare-adjacent role, with meaningful upside over 3-5 years by moving into senior CRC, site lead, or CRA/monitoring positions. Exact figures depend on the CRO, sponsor and location and are not stated in this posting.
Clinical license
Not required
Applicant reach
broad
Seniority
entry
Employment type
–
Date found
2026-10-24
Intelligence details
Flexible work details
- Eligible countries
- United States
Eligibility, licensing, and location restrictions can change. Always confirm details on the source posting before applying.
Why this is worth applying to
Worth considering if you are in or can relocate to Kansas City and want a recognised entry point into the clinical research/CRO industry. Request the full job description before applying, since no duties or requirements were provided here.
Who should apply
Nurses, pharmacists, IMGs, allied health professionals and healthcare graduates in the Kansas City area who want to move into industry-sponsored clinical research; also doctors exploring a research-operations path before deciding on CRA or medical affairs.
CV angle
Reframe real clinical work into trial-site language: patient screening and eligibility assessment, obtaining informed consent, protocol and SOP adherence, source documentation and EDC data entry, adverse event identification and reporting, maintaining regulatory binders, and coordinating multi-disciplinary teams. Quantify what you genuinely did — number of patients consented, studies or audits supported, documentation accuracy — and never claim GCP certification or monitoring experience you do not hold.
Skills to highlight
- Patient screening and recruitment
- Informed consent process
- Protocol and SOP adherence
- Source documentation and EDC data entry
- Adverse event identification and reporting
- Regulatory binder / essential document management
- Cross-functional coordination with investigators and sponsors
- Attention to detail and audit readiness
Role summary
Site-level coordinator for IQVIA-run or IQVIA-supported clinical trials in Kansas City, responsible for screening and consenting participants, scheduling study visits, collecting and entering trial data, maintaining regulatory documentation and supporting monitor visits — an on-site, operations-focused research role rather than a treating-clinician post.
We publish our own intelligence summary, never the full job description. Always confirm details with the employer when you apply.