Clinical Research Coordinator, On-Site

IQVIA LLC; Kansas City (MO); On-site; USD 38,000 - 95,000; Full time

Benefits offered by this job

Incentives

Health benefits

Job summary

IQVIA is seeking a Clinical Research Coordinator to join Avacare, a dynamic SMO that provides CRCs with exposure to diverse trials and hands-on responsibilities. You will recruit patients, obtain informed consent, manage regulatory documentation, and support site audits within a collaborative team.

Ideal candidates have 1–3 years CRC experience (CRC II up to 3 years), hands-on skills in vital signs, phlebotomy, ECGs, CTMS/eCRFs, and proficiency with Microsoft Office.

Qualifications

• CRC I: 1–3 years in clinical research at a site with participants.
• CRC II: 3+ years as a CRC at a clinical investigative site.
• Hands-on skills: vital signs, phlebotomy, ECGs, lab processing.
• CTMS/eCRFs and MS Office proficiency required.

Responsibilities

• Recruit patients and obtain informed consent.
• Manage regulatory documentation and site approvals.
• Coordinate trial activities across sites and monitors.
• Support audits and close-out activities.

Skills

Clinical skills

Site operations

Communication

Tools

CTMS

eCRFs

Microsoft Office

Job description

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. 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.
• Experience: 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.

Compensation & Benefits

The potential base pay range for this role, when annualized, is $37,800.00 - $94,500.00.

• 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.

Equal Opportunity

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.

Company Information

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.

Thank you for your interest in growing your career with us.