Benefits:

Health insurance

Opportunity for advancement

Paid time off

Training & development

Employment Type: Full‑time Experience Required: 1+ year independently managing clinical studies (Required) Languages: Fluent in English and Spanish (required)

About the Role

We’re seeking a Bilingual Clinical Research Coordinator who can independently manage clinical studies from start to finish. This role is ideal for someone who has already served as the primary coordinator on their own protocols—handling regulatory tasks, participant coordination, data quality, and study operations with minimal oversight. You’ll work closely with investigators, sponsors, and participants to ensure studies run smoothly, ethically, and in full compliance with GCP and IRB requirements.

Key Responsibilities

Serve as the primary coordinator for assigned clinical studies, managing all day‑to‑day operations.

Conduct participant recruitment, screening, informed consent, and study visits in both English and Spanish.

Maintain regulatory documentation, including IRB submissions, continuing reviews, amendments, and protocol deviations.

Coordinate study start‑up activities, including site initiation, training, and logistics.

Manage data entry, query resolution, and source documentation to ensure accuracy and audit readiness.

Communicate with sponsors, CROs, monitors, and internal teams to support study timelines and deliverables.

Ensure compliance with GCP, FDA regulations, and institutional policies.

Support budgeting, invoicing, and tracking of study‑related expenses when applicable.

Required Qualifications

Bilingual fluency in English and Spanish (verbal and written).

1+ year of experience independently coordinating clinical research studies, including direct responsibility for study visits and regulatory tasks.

Strong understanding of GCP, human subjects' protection, and clinical research workflows.

Excellent communication, organizational, and problem‑solving skills.

Ability to work with diverse patient populations and maintain professionalism in sensitive situations.

Proficiency with EMR systems, eCRFs, and common research platforms (e.g., CTMS tools).

Preferred Qualifications

Experience with FDA‑regulated trials (drug or device).

Certification such as CCRC, CCRA, or SOCRA/ACRP eligibility.

Experience in community‑based or multilingual research settings.

Phlebotomy skills or willingness to train.

What We Offer

Competitive compensation and benefits

Opportunities for professional development and certification

A collaborative, mission‑driven research environment

The chance to contribute to studies that directly impact patient care and health outcomes