Clinical Research Coordinator [Bilingual]

Rovia

  • Miami, Florida
  • 14 days ago

    Highlights

    The Clinical Research Coordinator (CRC) is responsible for coordinating and executing clinical trials in accordance with study protocols, ICH/GCP guidelines, sponsor requirements, and Rovia SOPs. This role partners closely with site teams to support study startup, enrollment, data quality, and overall study success.

    Numbers & Facts

    LocationMiami, Florida

    Description

    Position Summary:

    The Clinical Research Coordinator (CRC) is responsible for coordinating and executing clinical trials in accordance with study protocols, ICH/GCP guidelines, sponsor requirements, and Rovia SOPs. This role partners closely with site teams to support study startup, enrollment, data quality, and overall study success.

     

    Key Responsibilities:

    • Conducts and coordinates patient visits in accordance with study protocols.
    • Performs clinical tasks such as vital signs, EKGs, specimen collection and processing, and phlebotomy as applicable.
    • Ensures informed consent is properly obtained and documented.
    • Educates and guides participants through the study, ensuring a positive patient experience.
    • Monitors subject safety, reports adverse events, and escalates concerns as appropriate.
    • Completes timely and accurate source documentation and EDC data entry.
    • Resolves data queries and ensures data integrity.
    • Maintains investigational product accountability and proper storage and handling.
    • Prepares for and supports monitoring visits, audits, and inspections.
    • Collaborates with site staff and investigators to ensure protocol adherence and efficient visit flow.
    • Perform other duties as assigned.

    Skills/Abilities:

    • Strong knowledge of medical terminology and clinical procedures.
    • Understanding of ICH/GCP and regulatory requirements.
    • Excellent organizational skills and attention to detail.
    • Strong interpersonal and patient-facing communication skills.
    • Ability to multitask and manage competing priorities in a fast-paced environment.
    • Proficiency in Microsoft Office, EDC, and CTMS applications.
    • Ability to work both independently and collaboratively.
    • High level of professionalism and commitment to patient confidentiality.
    • Fluent in English and Spanish.

    Education/Experience:

    • High school diploma required, bachelor’s degree in related field preferred.
    • 2+ years of clinical research experience.
    • Experience with patient-facing activities (phlebotomy, vital signs, EKGs, etc.) strongly preferred.

    Similar Jobs