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    Senior Programmer - London, United Kingdom - ProPharma Group

    ProPharma Group
    ProPharma Group London, United Kingdom

    Found in: Jooble UK O C2 - 2 days ago

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    Description
    Senior Clinical Programmer page is loaded Senior Clinical Programmer

    Apply locations London time type Full time posted on Posted Yesterday job requisition id JR 3395 For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies.

    As the world's largest RCO (Research Consulting Organization), ProPharma partners with its clients through an advise-build-operate model across the complete product lifecycle.

    With deep domain expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners' most high-profile drug and device programs.

    Complete Clinical programmer tasks for assigned studies under minimal supervision according to the study contract and applicable SOPs.
    Design, develop, implement, maintain, and support clinical database systems.
    Code, test, and document databases as per programming standards and clinical validation policies.
    Program database manipulation and conduct data transfers for clients.
    Review Data Validation Plans and Case Report Forms as per area of expertise.

    Add all external data sources such as PK and central lab within the clinical database if integration is requested or required.

    Serve as programming contact to handle database issues within area of expertise.
    Support development and implementation of new technologies.
    Support Information Technology to evaluate new technology upgrades by participating in software change controls.
    Support development, revision and maintenance of core operating procedures and working instructions pertaining to database development, user acceptance testing and change controls
    Interface with project team to organize responsibilities and deliverables.
    Interface with Clinical Data Management and corporate team to negotiate timelines.
    Follow and influence the development of data standards and strategies pertaining to the standards library
    We are committed to diversity, equity, and inclusion. Please, no phone calls or emails to anyone regarding this posting.**
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