Clinical Research Associate II or Senior Clinical Research Associate - Harrow - Parexel

    Parexel
    Parexel Harrow

    4 days ago

    Description

    Clinical Research Associate II or Senior Clinical Research Associate


    Parexel Uxbridge, England, United Kingdom

    Parexel is in the business of improving the world's health. We do this by providing a suite of biopharmaceutical services that help clients across the globe transform scientific discoveries into new treatments. From clinical trials to regulatory, consulting, and market access, our therapeutic, technical, and functional ability is underpinned by a deep conviction in what we do. We believe in our values, Patients First, Quality, Respect, Empowerment & Accountability.

    What You'll Do

    • Leverage your expertise. Conduct qualification visits (QV), site initiation visits (SIV), monitoring visits (MV) and termination visits (TV) at assigned clinical sites and generate visit/contact reports.
    • Build relationships. Oversee integrity of the study and utilize problem‑solving skills to promote rapport with the site and staff.
    • Protect patients. Review the performance of the trial at designated sites, ensure the rights and well‑being of human subjects are safeguarded and are in accordance with protocol.
    • Drive productivity. Develop patient recruitment strategies in conjunction with the clinical site to meet enrollment timelines, while also ensuring compliance with the approved standard operating procedures (SOPs), protocol/amendment(s), GCP, and the applicable regulatory requirement(s).
    • Ensure quality. Evaluate the quality and integrity of the reported data, site efficacy and drug accountability.
    • Execute. Monitor the completeness and quality of Regulatory Documentation and perform site document verification.

    More About You

    • Site Management or equivalent experience in clinical research, with understanding of clinical trials methodology and terminology.
    • Ability to perform all clinical monitoring activities independently.
    • Bachelor's or equivalent degree in biological science, pharmacy or other health related discipline.
    • Strong interpersonal, written, and verbal communication skills within a matrixed team.
    • Experience working in a self‑driven capacity, with a sense of urgency and limited oversight.
    • A client‑focused approach to work and flexible attitude with respect to assignments/new learning.
    • The ability to manage multiple tasks, evaluate a variety of unpredictable scenarios and achieve project timelines while being able to apply your understanding of study protocol(s).
    • An honest and ethical work approach to promote the development of life‑changing treatments for patients.
    • Strong computer skills, including but not limited to the knowledge of a Clinical Trial Management System (CTMS), Electronic Document Management System (EDMS) and MS‑Office products such as Excel and Word.

    Seniority level


    Entry level

    Employment type


    Full‑time

    Job function


    Health Care Provider, Science, and Research

    Industries


    Pharmaceutical Manufacturing, Biotechnology Research, and Hospitals and Health Care


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