Phase 1 Clinical Research Coordinator

Barrington James Limited; Town of Florida (NY); On-site; USD 52,000 - 78,000; Full time

Job summary

Barrington James Limited is seeking a Clinical Research Coordinator for our Miami, FL site to own the full study lifecycle from startup through closeout. You will coordinate Phase I trials, screen and enroll subjects, and perform key procedures across a high-volume pharmacology unit.

Ideal candidates have hands-on Phase I experience, bilingual English/Spanish, and are based in or willing to work on-site full-time in Miami. US work authorization is required.

Qualifications

• Hands-on clinical research coordination in Phase I/healthy volunteers.
• Strong communication skills in Spanish and English.
• On-site, full-time in Miami, FL; US work authorization required.

Responsibilities

• Coordinate trials from protocol review through closeout.
• Screen/enroll subjects, obtain consent, manage visits.
• Perform vitals, ECGs, phlebotomy; support PK sampling.
• Manage EDC data entry and source documentation.
• Track and report adverse events per protocol.
• Liaise with PIs, sponsors and CROs.
• Support monitoring visits and manage investigational product.

Skills

Phase I experience

Bilingual English/Spanish

EDC systems

Study coordination

Attention to detail

Tools

EDC software

Job description

A leading early-phase clinical research site in Miami is seeking a Clinical Research Coordinator to join a fast-paced, high-volume clinical pharmacology unit. This is a hands-on role coordinating Phase I and early-phase studies from startup through closeout, ideal for someone who wants ownership over the full study lifecycle, not just paperwork.

What you'll do:

• Coordinate clinical trials from protocol review through study closeout
• Screen and enroll subjects, obtain informed consent, and manage study visits
• Perform clinical procedures (vitals, ECGs, phlebotomy) and support PK sampling
• Manage EDC data entry, source documentation, and query resolution
• Track and report adverse events per protocol requirements
• Liaise directly with Principal Investigators, sponsors, and CROs
• Support monitoring visits and manage investigational product per protocol

Requirements:

• Hands-on clinical research coordination experience in Phase I / healthy volunteer studies
• Strong Communication skillsin Spanish and English
• Confident working with protocols, informed consent, and EDC systems
• Detail-oriented, comfortable operating independently
• Must be based in or willing to work on-site full-time in Miami, FL
• Applicants must be currently authorized to work in the United States on a full-time basis. We are unable to sponsor employment visas for this role.