Clinical Research Coordinator, On-Site

IQVIA; Kansas City (MO); Sur place; USD 37 800 - 94 500; Plein temps

Résumé du poste

IQVIA is seeking a Clinical Research Coordinator on-site in Kansas City, MO. You will manage trial activities, recruit patients, obtain informed consent, and maintain regulatory documents in a collaborative, fast-paced environment.

You will work with investigators, sponsors, and monitors to ensure study milestones are met while maintaining high data quality and patient safety. This role offers exposure to diverse trials and a pathway toward advanced clinical operations responsibilities.

Qualifications

• Hands-on CRC experience at a clinical site with patients.
• Experience across multiple trials and regulatory documentation.
• Proficiency with CTMS, eCRFs, and MS Office.

Responsabilités

• Coordinate patient recruitment and informed consent.
• Ensure regulatory documentation and site audits.
• Collaborate with investigators, sponsors, and monitors.
• Manage trials across multiple therapeutic areas.

Connaissances

Vital signs

Phlebotomy

ECGs

Lab processing

Outils

CTMS

eCRFs

Microsoft Office

Description du poste

## Clinical Research Coordinator, On-SiteApplylocations: Kansas City, MO, United States of Americatime type: Full timeposted on: Posted Todayjob requisition id: R1555940Are you ready to accelerate your career in clinical research? Join Avacare, a dynamic Site Management Organization (SMO) where Clinical Research Coordinators (CRCs) gain unparalleled exposure to diverse trials, hands-on responsibilities, and a collaborative team environment.**Why Avacare?** At Avacare, CRCs wear more hats than in traditional research settings. You’ll gain experience across multiple therapeutic areas, manage complex protocols, and take ownership of key trial activities — from patient recruitment and informed consent to regulatory documentation and site audits. This breadth of responsibility not only strengthens your core CRC skills but also prepares you for future roles in clinical operations, monitoring, and beyond.**What You’ll Gain:**Broadened Skill Set: Manage 2–6 trials of varying complexity, perform clinical procedures, and lead study coordination from start to finish. Professional Growth: Work closely with investigators, sponsors, and monitors while mentoring junior staff and contributing to internal training. Collaborative Culture: Be part of a supportive team that values initiative, adaptability, and continuous learning. Global Impact: Experience the synergy of working within a local SMO backed by the resources and reach of a global CRO.**Qualifications:** Clinical Skills: Hands-on experience in obtaining vital signs, performing phlebotomy, conducting ECGs, and processing lab specimens. Site Operations Knowledge: Solid understanding of site operations and the drug development process.**Experience:** CRC I: Minimum of 1-3 years in clinical research setting at a clinical investigative site working with participants. CRC II: Minimum of 3 years as a Clinical Research Coordinator in a clinical investigative site working with participants. Communication & Documentation: Strong written and verbal communication skills, with attention to detail and time management. Technical Proficiency: Comfortable using CTMS, eCRFs, and Microsoft Office tools.Whether you're early in your CRC journey or ready to take the next step, Avacare offers a unique environment where your contributions matter and your career can flourish.IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.comIQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoeIQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.The potential base pay range for this role, when annualized, is $37,800.00 - $94,500.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.