Clinical Research Coordinator - Albuquerque, NM

• 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. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide. To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us. EEO Minorities/Females/Protected Veterans/Disabled