Spanish Bilingual Clinical Research Coordinator - Dorado, Puerto Rico

IQVIA • San Juan, PR

1d • Onsite

About The Position

IQVIA is seeking a Spanish Bilingual Clinical Research Coordinator (CRC) to support clinical research studies conducted under the supervision of a Principal Investigator. This hands-on role is ideal for a detail-oriented professional with prior coordinating experience who is comfortable working directly with patients, managing study data, and ensuring strict adherence to study protocols and Good Clinical Practice (GCP). The CRC plays a critical role in the day-to-day execution of clinical trials, patient safety, and data integrity.

Requirements

• Bachelor’s degree preferred, or an equivalent combination of education and relevant experience
• Minimum of 1+ year of hands-on clinical research coordinating experience
• Demonstrated experience with: Patient-facing study visits, EDC data entry and query resolution, Patient recruitment and screening, Investigational Product (IP) accountability, Source document and chart review
• Working knowledge of clinical trials, GCP, and medical terminology
• Strong attention to detail with the ability to manage multiple priorities
• Ability to build effective working relationships with study teams and participants
• Fluency in Spanish required (spoken and written); English proficiency preferred
• Comfortable working on-site and independently within a structured research environment

Responsibilities

• Conduct and support participant visits, including clinical procedures such as ECGs, vital signs, and biological sample collection
• Coordinate study activities in compliance with protocols, GCP, and regulatory requirements
• Prepare study materials, organize equipment, and support logistical planning for study visits
• Assist with patient recruitment, screening, consent, and visit coordination
• Perform accurate electronic data capture (EDC) entry, query resolution, and source documentation
• Maintain investigational product (IP) accountability, including reconciliation and documentation
• Conduct chart reviews to support eligibility determination and data verification
• Collaborate closely with investigators, sponsors, and monitors to resolve study issues and maintain data quality
• Serve as a patient advocate, ensuring participant safety, comfort, and confidentiality
• Uphold Health & Safety and quality standards across all study activities

Benefits

• Health insurance
• Dental insurance
• Vision insurance

What This Job Offers

• Job Type: Part-time
• Career Level: Mid Level
• Education Level: Associate degree
• Number of Employees: 5,001-10,000 employees