Clinical Trial Research Assistant

Advanced Rheumatology of Houston
  • Spring, TX
    Today

    Job Description

    Job Description

    Job Description
    Clinical Trial Research Assistant
    The Woodlands, TX | Full-Time | Private Outpatient Medical Clinic/Onsite

    Woodlands Private Outpatient Medical Clinic is actively seeking a Clinical Trial Research Assistant to join our dedicated clinical research team. This is an exciting opportunity to be involved in cutting-edge medical research in a supportive and dynamic outpatient setting.

    Key Responsibilities:
    • Process and ship biological specimens per study protocol.
    • Maintain lab inventory and order clinical trial supplies.
    • Ensure accurate and complete study documentation in compliance with institutional and federal regulations.
    • Support research coordinators with testing procedures and overall trial conduct.
    • Advertise, screen, recruit, and enroll patients in clinical trials.
    • Obtain informed consent and explain study participation clearly.
    • Schedule appointments, diagnostic tests, and study-related procedures.
    • Assist with data entry into electronic case report forms (eCRFs) and databases.
    • Support the preparation and submission of reports to regulatory bodies (IRB, FDA, DSMB).
    • Maintain knowledge of current study protocols and standard operating procedures.
    • Prepare for monitoring visits, sponsor audits, and regulatory inspections.
    • Help collect and report adverse events.
    • Attend ongoing training and continuing education relevant to research duties.

    Preferred Skills:
    • Phlebotomy, ECG/EKG, and vital signs collection preferred (or willingness to be trained).
    • Experience with specimen processing, shipping, and documentation.
    • Bilingual (English/Spanish) is a plus.

    Requirements:
    • Bachelor's degree or higher in a science-related field US University (e.g., biology, chemistry, biochemistry).
    • Previous lab experience with biological specimen handling.
    • Proficient in maintaining documentation and adhering to study protocols.
    • MUST live within 30 mins of The Woodlands.
    • THIS POSITION IS ONSITE.
    • Must be Technologically Adept.
    • Strong attention to detail and protocol compliance.
    • Excellent communication and organizational skills.

    Why Join Us?
    • Supportive, collaborative team environment.
    • Opportunity to work on innovative, impactful clinical trials.
    • On-the-job training and professional development.
    • Regular weekday schedule with no night or weekend shifts.

    Numbers & Facts

    LocationSpring, TX

    Skills

    • Adverse Eventsunmatched
    • Biochemistryunmatched
    • Biological Processesunmatched
    • Biologyunmatched
    • Calendar Managementunmatched
    • Case Report Form (CRF)unmatched
    • Chemistryunmatched
    • Clinical Assessmentunmatched
    • Clinical Researchunmatched
    • Clinical Trialunmatched
    • Communication Skillsunmatched
    • Data Entryunmatched
    • Detail Orientedunmatched
    • Documentationunmatched
    • Electrocardiogramunmatched
    • English Languageunmatched
    • FDA (Food and Drug Administration)unmatched
    • Federal Laws and Regulationsunmatched
    • IRB/IEC (Institutional Review Board/Independent Ethics Committee)unmatched
    • Informed Consentunmatched
    • Inventory Managementunmatched
    • Laboratoryunmatched
    • Medical Productsunmatched
    • Medical Researchunmatched
    • Multilingualunmatched
    • Order Suppliesunmatched
    • Organizational Skillsunmatched
    • Outpatient Careunmatched
    • Phlebotomyunmatched
    • Regulationsunmatched
    • Regulatory Reportsunmatched
    • Research Protocolsunmatched
    • Sample/Specimen Processingunmatched
    • Shipping Documentsunmatched
    • Spanish Languageunmatched
    • Standard Operating Procedures (SOP)unmatched
    • Team Playerunmatched
    • Testingunmatched

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