Bilingual Clinical Research Coordinator

Puerto-Rico-Science-Technology-; San Juan (PR); On-site; USD 42,000 - 60,000; Full time

Job summary

The Puerto Rico Consortium for Clinical Investigation (PRCCI) seeks a Clinical Research Coordinator in San Juan, PR to support study start-up, regulatory compliance, and day-to-day trial operations.

You will coordinate regulatory submissions, develop study documents, identify and enroll participants, manage data, and liaise with investigators, sponsors, and clinical staff to ensure timely, accurate trial execution.

Qualifications

• BA/BS in health-related field or 3+ years in clinical trials.
• Proven work experience as a Clinical Research Coordinator.
• Excellent written and verbal English/Spanish communication.
• Ability to learn and apply NIH/FDA/ICH-GCP guidelines.
• Strong organizational and multitasking capabilities.

Responsibilities

• Coordinate study start-up activities, including regulatory submissions (IRB/IEC).
• Develop and maintain source documents, CRFs, study binders, and SOPs.
• Ensure NIH, FDA, ICH-GCP compliance and institutional guidelines.
• Identify, screen, and recruit eligible participants per protocol.
• Obtain informed consent and document procedures.
• Schedule visits, collect data, and manage specimens as required.
• Maintain regulatory documents and prepare for monitoring visits.
• Track study expenses and assist with budget management.
• Serve as liaison between investigators, sponsors, and staff.
• Train site staff on protocol, procedures, and compliance.

Skills

Bilingual English/Spanish

Regulatory compliance

Communication skills

Project coordination

Time management

Education

BA/BS in health-related field

Advanced degree desirable

Tools

Microsoft 365 Suite

SharePoint

Google Workspace

Docusign

Zoom

Job description

The Puerto Rico Consortium for Clinical Investigation (PRCCI) seeks a Clinical Research Coordinator in San Juan, PR to support study start-up, regulatory compliance, and day-to-day trial operations.

You will coordinate regulatory submissions, develop study documents, identify and enroll participants, manage data, and liaise with investigators, sponsors, and clinical staff to ensure timely, accurate trial execution.