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Clinical Research Coordinator, On-Site, Kansas City, MO
Clinical Research Coordinator, On-Site, Kansas City, MOIQVIA • Kansas City, Kansas, USA
Clinical Research Coordinator, On-Site, Kansas City, MO

Clinical Research Coordinator, On-Site, Kansas City, MO

IQVIA • Kansas City, Kansas, USA
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Are 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. Youll 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 Youll Gain :

Broadened Skill Set : Manage 26 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 youre 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

IQVIA 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. potential base pay range for this role when annualized is $36600.00 - $91300.00. 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.

Required Experience :

IC

Key Skills

Experience Working With Students,Google Docs,Organizational skills,Classroom Experience,Data Collection,Materials Handling,Workers' Compensation Law,OSHA,Special Operations,Team Management,Experience with Children,Supervising Experience

Employment Type : Full-Time

Experience : years

Vacancy : 1

Monthly Salary Salary : 36600 - 91300

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Clinical Research Coordinator • Kansas City, Kansas, USA

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