Medical Coding Lead - England - Proclinical Staffing

    Proclinical Staffing
    Proclinical Staffing England

    1 week ago

    Description

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    Senior Research Associate | Clinical Operations and Biometrics @ Proclinical Staffing

    We are on the hunt for bold, innovative thinkers who are ready to help push the boundaries of science and make a tangible difference in the world.

    Proclinical is seeking a Medical Coding Lead with a focus on oncology. This role involves strategic leadership and execution of medical coding activities for clinical trials, ensuring high-quality coded data that meets industry standards and regulatory requirements. You will be part of a small global team within the Biometrics Center of Excellence, contributing to the development and implementation of coding processes.

    This is a remote role based in London, the UK, or anywhere within the EU.

    Responsibilities:

    • Lead clinical trial coding deliverables and provide mentorship to team members.
    • Develop and implement long-term coding strategies for oncology trials.
    • Serve as a subject matter expert in oncology terminology and coding practices.
    • Oversee coding of clinical trial data, including adverse events and concomitant medications.
    • Review outsourced study-level coded data for quality and consistency.
    • Maintain coding conventions and guidelines across studies.
    • Manage queries related to unclear terminology or posology in data.
    • Collaborate with data management and clinical development teams to optimize workflows.
    • Maintain effective communication with stakeholders, including vendors and trial sites.
    • Develop and manage dictionary processes, focusing on oncology-specific terms.
    • Utilize medical dictionaries like MedDRA and WHODrug effectively.

    Key Skills and Requirements:

    • Degree in health science-related field (e.g., biology, pharmacy, nursing).
    • Certification in clinical coding preferred (e.g., CCC, CPC).
    • Extensive experience in medical dictionary coding, especially in oncology.
    • Advanced knowledge of ICH-GCP guidelines and drug development regulations.
    • Strong understanding of oncology trial design and execution.
    • Expertise in medical terminology, particularly oncology-related terms.
    • Experience with clinical trial data systems and EDC coding tools; Medidata Coder preferred.
    • Ability to manage multiple trials and tasks efficiently in a dynamic environment.
    • Excellent communication and organizational skills.
    • Fluent in English, both written and spoken.
    • Ability to work independently and collaboratively in a team setting.

    If you are having difficulty in applying or if you have any questions, please contact Erin Magalie at

    Apply Now:

    If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists please request a call back at the top of this page.

    Proclinical is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Proclinical is acting as an Employment Agency in relation to this vacancy.

    By submitting this application, you confirm that you've read and understood our privacy policy, which informs you how we process and safeguard your data -

    Seniority level

    • Seniority level

      Mid-Senior level

    Employment type

    • Employment type

      Full-time

    Job function

    • Job function

      Science

    • Industries

      Professional Services

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