Clinical Research Coordinator: NIH Trials & Study Ops

PRCCI; San Juan (PR); On-site; USD 45,000 - 65,000; Full time

Job summary

PRCCI is seeking a Clinical Research Coordinator in San Juan, PR to support study startup, participant recruitment, and data management for NIH/FDA-aligned trials. The role ensures regulatory compliance, documentation accuracy, and effective collaboration with investigators and sponsors.

The position is a fixed-term contract (1 year) reporting to the Associate Director, with responsibilities spanning study coordination, data handling, and regulatory support in a fast-paced environment.

Qualifications

• Excellent written and verbal communication in English and Spanish.
• Strong customer service and interpersonal skills for clients and participants.
• Ability to work collaboratively in a dynamic, fast-paced environment.
• Proficient with Microsoft 365 Suite, Google apps, SharePoint, OneDrive, Dropbox, Adobe PDF, Docusign, Zoom.
• Willing to learn new processes and company-specific software.
• Occasionally, after-hours work may be required.

Responsibilities

• Coordinate study startup activities, including regulatory submissions (IRB/IEC) and site initiation.
• Identify, screen, and recruit eligible participants according to protocol criteria.
• Schedule visits, collect data, and manage study documentation and SOPs.
• Maintain regulatory documents and support monitoring visits, audits, and inspections.

Skills

Bilingual English/Spanish

Excellent communication

Team collaboration

Time management

Adaptability

Willingness to learn

Education

BA/BS in health-related field

Clinical trials experience (3+ years)

Tools

Microsoft 365 Suite

SharePoint

OneDrive

Dropbox

Adobe PDF

Docusign

Zoom

Job description

PRCCI is seeking a Clinical Research Coordinator in San Juan, PR to support study startup, participant recruitment, and data management for NIH/FDA-aligned trials. The role ensures regulatory compliance, documentation accuracy, and effective collaboration with investigators and sponsors.

The position is a fixed-term contract (1 year) reporting to the Associate Director, with responsibilities spanning study coordination, data handling, and regulatory support in a fast-paced environment.