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    Medical Writer Remote - United Kingdom - MMS Holdings Inc

    MMS Holdings Inc
    MMS Holdings Inc United Kingdom

    3 weeks ago

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    Description

    MMS is an innovative, data-focused CRO that supports the pharmaceutical, biotech, and medical device industries with a proven, scientific approach to complex trial data and regulatory submission challenges.

    Strong industry experience, technology-enabled services, and a data-driven approach to drug development make MMS a valuable CRO partner, creating compelling submissions that meet rigorous regulatory standards.

    With a global footprint across four continents, MMS maintains a 97 percent customer satisfaction rating, and the company has been recognized as a leading CRO inGlobal Health & Pharma'sinternational awards programs for the last three consecutive years.

    Under minimal supervision, the Medical Writer will critically evaluate, analyze, and interpret the medical literature to select primary resource materials for adequate study design, statistical significance, scientific rigor and absence of bias
    5 documents, presentation materials and publications to medical journals
    Complete writing assignments in a timely manner
    Maintain timelines and workflow of writing assignments
    Highly proficient with styles of writing for various regulatory documents
    Interact directly and independently with client to coordinate all facets of projects; competent communicator skills for projects
    Take ownership of a given assignment, proactively consulting other project team members and other department representatives for information or guidance as necessary
    Mentor medical writers and other members of the project team who are involved in the writing process
    At least 3 years of previous experience in the pharmaceutical industry
    Must have at least 3-5 years of industry regulatory writing and clinical medical writing experience
    The ideal candidate would hold a Bachelors, Masters, or Ph.
    D. in scientific, medical, clinical discipline
    Experience leading and managing teams while authoring regulatory documents with aggressive timelines
    Experience in regulatory submissions (clinical study reports) presented to regulatory authorities a plus
    Understanding of clinical data
    Exceptional writing skills are a must
    Candidate must be an expert in MS Word, Excel, PowerPoint, and related word processing tools
    Experience being a project lead, or managing a project team
    Experience leading and managing teams while authoring regulatory documents with aggressive timelines
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