Spanish Bilingual Clinical Research Coordinator - Lancaster, CA

IQVIA • Parsippany, NJ

1d • $35 - $42 • Onsite

About The Position

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.

Requirements

• 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.

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.

What This Job Offers

• Job Type: Part-time
• Career Level: Entry Level
• Number of Employees: 5,001-10,000 employees