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