Job Title: CRC

Work Location: Palm Beach County, Florida

Summary:

Seeking an experienced, bilingual (Spanish/English) Clinical Research Coordinator to support a high-volume cardiology research site. The role requires strong clinical skills, the ability to work independently, and effective communication with physicians and sponsors. The position involves managing multiple studies in a fast-paced environment, ensuring regulatory compliance, and supporting all aspects of clinical trial coordination.

Responsibilities:

• Oversee all phases of clinical trial activities, from participant screening to study closeout, across a diverse cardiology protocol portfolio.
• Conduct informed consent discussions and eligibility assessments in both Spanish and English to ensure participant understanding and compliance.
• Serve as a primary liaison with investigators, sponsor representatives, and clinical research associates, maintaining professionalism and expertise.
• Maintain regulatory binders, source documentation, and perform accurate data entry into electronic data capture (EDC) systems.
• Schedule and conduct study visits, including the collection and processing of biological samples according to protocol requirements.
• Work autonomously in a high-volume, fast-paced environment with minimal supervision, demonstrating strong organizational skills.
• Ensure adherence to ICH-GCP guidelines, IRB requirements, and sponsor standard operating procedures throughout all study activities.
• Support concurrent enrollment and follow-up activities for multiple ongoing clinical studies, ensuring timely and accurate execution of study tasks.

Qualifications:

• Bilingual fluency in Spanish and English, both written and spoken (required).
• Minimum of 2 years of hands-on clinical research coordination experience at a research site.
• Strong knowledge of Good Clinical Practice (GCP), FDA regulations, and protocol compliance.
• Experience working in a high-volume or multi-study site environment.
• Ability to work directly with physicians and sponsor/CRA personnel.
• Proficiency with electronic data capture (EDC) platforms and study management documentation.
• ACRP or SOCRA certification (CCRC, CCRP) preferred.
• Background in cardiology or cardiovascular research is a strong plus.

Published Category: Clinical Operations & Development