Clinical Research Coordinator

IQVIA Argentina; Scottsdale (AZ); On-site; USD 38,000 - 95,000; Full time

Job summary

IQVIA is seeking a fully on-site Clinical Research Coordinator in Scottsdale, Arizona. You will gain exposure across multiple trials, manage procedures, and coordinate study activities from recruitment to regulatory documentation.

Ideal candidates have hands-on clinical skills and experience with CTMS/eCRFs, plus strong communication and time management. This role offers growth within a global CRO network and collaborative culture.

Qualifications

• Hands-on skills: vital signs, phlebotomy, ECGs, lab specimen processing.
• Solid understanding of site operations and drug development processes.
• CRC progression: CRC I 1–3 years; CRC II 3+ years at a clinical site.

Responsibilities

• Coordinate 2–6 trials of varying complexity, lead study coordination from start to finish.
• Collaborate with investigators, sponsors, and monitors; mentor junior staff.
• Support regulatory documentation and site audits; ensure compliance and data integrity.

Skills

Vital signs

Phlebotomy

ECGs

Lab specimen processing

Site operations

Communication

Documentation

Time management

Tools

CTMS

eCRFs

Microsoft Office

Job description

This is a fully on-site position in Scottsdale, Arizona

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.
  • 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.

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.com

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. https://jobs.iqvia.com/eoe

IQVIA 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.