Clinical Research Coordinator - Albuquerque, NM
Work Set‑Up: On‑site
Schedule: 24 Hours/Week (Part‑time)

About IQVIA

IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services. We collaborate with leading pharmaceutical, biotechnology, and medical device organizations to advance innovation and improve patient outcomes worldwide. Through scientific expertise, operational excellence, and cutting‑edge technology, IQVIA is shaping the future of healthcare.

About the Role

IQVIA is seeking a Clinical Research Coordinator (CRC) to support clinical research studies conducted under the supervision of a Principal Investigator. This role is well‑suited for a detail‑oriented research professional who enjoys direct patient interaction, values data integrity, and is committed to high‑quality clinical research within diverse communities.

As a CRC, you will play a critical role in coordinating study operations, supporting patient recruitment and retention, performing study‑related procedures, and ensuring adherence to study protocols and regulatory requirements.

Key Responsibilities

Coordinate and conduct clinical research activities in accordance with study protocols, Good Clinical Practice (GCP), and applicable regulatory requirements
Perform study‑related clinical procedures, including ECGs, vital signs, and biological sample collection
Conduct patient visits including screening, enrollment, education, orientation, and follow‑up
Support patient recruitment efforts and community outreach, including bilingual (English/Spanish) communication
Prepare study materials, manage equipment setup, and support daily clinic operations
Accurately collect, document, and enter clinical data into electronic data capture (EDC) systems and case report forms (CRFs)
Request, review, and manage medical records to support study eligibility and documentation
Collaborate with investigators, sponsors, and monitors to address data queries and ensure study quality
Maintain a safe clinical environment and serve as a patient advocate throughout study participation

Qualifications

Bachelor’s degree preferred, or an equivalent combination of education and relevant experience
Minimum of 1+ year of clinical research coordination experience, including prior study coordination
Hands‑on experience with clinical research operations, including:
- Data entry and query resolution in EDC systems
- Chart pre‑screening and patient pre‑screening activities
- Conducting and coordinating patient visits
- Patient outreach and education via phone and face‑to‑face communication regarding clinical trials
- Scheduling study visits and managing visit logistics
- Collection, processing, and shipping of laboratory samples
- Recruitment activities and participant follow‑up
- Regulatory document review and maintenance
Working knowledge of clinical trial processes, GCP guidelines, and medical terminology
Experience requesting and managing medical records
Bilingual in English and Spanish (written and verbal) is preferred but not required
Strong organizational skills, attention to detail, and ability to work effectively with diverse teams and patient populations

Ready to Make an Impact?

Join IQVIA and contribute to high‑quality clinical research that advances science while serving diverse patient communities.
Apply today and be part of a team helping bring innovative treatments to patients.

Additional Information

This position is not eligible for visa sponsorship

#LI-CES #LI-DNP #LI-HCP #ONSITE

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 is $35.00-$42.00 per hour. 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.