About IQVIA

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

About the Role

We are seeking a Spanish‑Bilingual Clinical Research Coordinator (CRC) to support the conduct of clinical research studies under the direction of a Principal Investigator. This role is ideal for a detail‑oriented professional with hands‑on clinical research experience who is passionate about patient care, data quality, and community engagement.

As a CRC, you will be responsible for coordinating study activities, performing clinical procedures, supporting patient recruitment, and ensuring compliance with study protocols and regulatory standards.

Key Responsibilities

• Coordinate and conduct clinical research activities in compliance with study protocols, Good Clinical Practice (GCP), and regulatory requirements.
• Perform clinical procedures, including ECGs, vital signs, and biological sample collection.
• Conduct patient visits, including screening, enrollment, orientation, and follow‑up.
• Support patient recruitment and community outreach initiatives, including bilingual (English/Spanish) communication.
• Prepare study materials, set up equipment, and support day‑to‑day study logistics.
• Collect, document, and enter clinical data accurately into electronic data capture (EDC) systems and case report forms (CRFs).
• Request and review medical records as required for study participation.
• Collaborate with investigators, sponsors, and monitors to address queries and ensure data quality.
• Maintain a safe clinical environment and act 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.
• Experience with patient recruitment, screening, and conducting study visits.
• Proficiency in data entry, EDC systems, and query resolution.
• 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) required.
• Strong attention to detail, organizational skills, and ability to work effectively with diverse teams and patient populations.

Additional Information

• This position is not eligible for visa sponsorship.

Interested in advancing clinical research while serving diverse communities?
Apply today to join IQVIA and contribute to high‑quality clinical studies that help bring new treatments to patients.