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    Clinical Research Coordinator - San Antonio, United States - Pinnacle Clinical Research

    Pinnacle Clinical Research
    Pinnacle Clinical Research San Antonio, United States

    3 weeks ago

    Default job background
    Full time
    Description
    Come be part of our team and make a difference as we pave the way into the future of liver medicine. Pinnacle Clinical Research is committed to conducting innovative research with a specific emphasis on fatty liver disease (non-alcoholic). Join us in the journey of discovery!

    Summary: PCR is in search of a Clinical Research Coordinator I to oversee the day-to-day operations of assigned clinical trials, assist in project planning, and ensure adherence to work scope, study protocol, and regulatory requirements. Responsibilities include engaging in meetings to promote studies, recruit and screen participants, as well as document and report on daily study operations and participant status. The ideal candidate must excel at multitasking, be detail-oriented, an effective communicator, and provide top-notch patient care. Collaboration with team members, pharmaceutical sponsors, and external vendors is essential. This role reports directly to the Clinical Research Project Manager.

    Duties and Responsibilities:
    • Exercise judgment within defined limits of clinical trial protocols and procedures.
    • Maintain subject and document confidentiality.
    • Complete assessments with patients as directed by the study.
    • Liaise with sponsors and vendors.
    • Prepare for study visits and inspections.
    • Conduct subject screening and recruitment.
    • Contribute to data management.
    • Improve patient care and satisfaction.
    • Interact with various personnel involved in the study.
    • Coordinate multiple projects based on protocol directives.
    • Attend study-related visits and meetings.
    Administration:
    • Complete electronic forms.
    • Prepare study-related correspondence.
    • Ensure timely entry of patient data.
    • Maintain and organize study documents.
    • Report safety information to regulatory agencies.
    • Understand and comply with regulatory requirements.
    • Perform quality checks on study documents.
    • Contribute to CAPA process as necessary.

    Responsibilities may vary, and new tasks may be assigned.

    Qualifications:
    • High school diploma required.
    • Bachelor's Degree in scientific field preferred.
    • Proficient in Microsoft Office and Clinical Research IO (CRIO) or equivalent CTMS.
    • Familiarity with ICH/GCP guidelines.
    • Training and certification in relevant areas.
    • Strong organizational and time management skills.
    • Excellent communication skills.
    • Knowledge of medical terminology.
    • Proficiency in Spanish and English.
    Competencies:
    • Effective communication skills.
    • Ability to work independently and in a team setting.
    • Strong people skills and ability to handle confidential matters.
    • Positive and professional demeanor.
    • Problem-solving and decision-making abilities.
    • Proactive and results-oriented.
    Work Environment and Physical Demands:
    • Work environment includes office/laboratory and clinical settings.
    • Exposure to biological materials.
    • Protective equipment required.
    • Occasional domestic/international travel.
    • Ability to perform job functions for extended periods.
    • Physical tasks may include lifting and mobility.
    Benefits of working at Pinnacle Clinical Research:
    • 401k.
    • Medical, dental, vision, and other insurance options.
    • Paid time off and holidays.
    • Wellness facilities in specific locations.
    • And more.

    Pinnacle Clinical Research is an equal opportunity employer. Applicants will be considered without regard to various factors.

    About Pinnacle Clinical Research:

    Pinnacle Clinical Research is dedicated to conducting innovative research with a focus on fatty liver disease. Our commitment to quality research complements the medical care offered to our volunteers. Join us in the journey of discovery!

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