Clinical Research Assistant

Rovia

  • Saint Charles, Missouri
  • 3 days ago
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    Skills

    • Adverse Eventsunmatched
    • Certified Medical Assistantunmatched
    • Clinical Assessmentunmatched
    • Clinical Researchunmatched
    • Clinical Trial Managementunmatched
    • Communication Skillsunmatched
    • Data Entryunmatched
    • Data Qualityunmatched
    • Detail Orientedunmatched
    • Documentationunmatched
    • Electrocardiogramunmatched
    • Electronic Data Capture (EDC)unmatched
    • GCP (Good Clinical Practices)unmatched
    • High School Diplomaunmatched
    • ICH Regulationsunmatched
    • Informed Consentunmatched
    • Interpersonal Skillsunmatched
    • Investigational New Drug (IND)unmatched
    • Maintain Complianceunmatched
    • Medical Terminologyunmatched
    • Medical Treatmentunmatched
    • Microsoft Officeunmatched
    • Multitaskingunmatched
    • Organizational Skillsunmatched
    • Patient Confidentialityunmatched
    • Phlebotomyunmatched
    • Regulatory Requirementsunmatched
    • Research Protocolsunmatched
    • Sample/Specimen Processingunmatched
    • Specimen Collectionunmatched
    • Standard Operating Procedures (SOP)unmatched
    • Startupunmatched
    • Time Managementunmatched

    Description

    Position Summary:

    The Clinical Research Assistant 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:

    • Conduct and coordinate patient visits in accordance with study protocols.
    • Perform clinical tasks such as vital signs, ECGs, specimen collection/processing, and phlebotomy (as applicable).
    • Ensure informed consent is properly obtained and documented.
    • Educate and guide participants throughout the study, ensuring a positive patient experience.
    • Monitor subject safety, report adverse events, and escalate concerns as appropriate.
    • Complete timely and accurate source documentation and EDC data entry.
    • Resolve data queries and ensure data integrity.
    • Maintain investigational product accountability and proper storage/handling.
    • Prepare for and support monitoring visits, audits, and inspections.
    • Collaborate 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.

    Education/Experience:

    • High school diploma required, bachelor’s degree in related field preferred.
    • 0-1 years of clinical research experience.
    • Experience with patient-facing activities (phlebotomy, vital signs, EKGs, lab processing, etc.) required.
    • Phlebotomy or Medical Assistant certification preferred.
    • Current IATA certification preferred.

    Position will require availability to start at 6:00AM.

    Numbers & Facts

    LocationSaint Charles, Missouri

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