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Nutley

    Clinical Programmer Analyst - Nutley, United States - Integrated Resources

    Integrated Resources
    Integrated Resources Nutley, United States

    3 weeks ago

    Default job background
    Description
    Qualifications
    100% Remote


    • Minimum 10 years of relevant work experience to include data management and/or database programming and spec Design activities including 10 years in Medidata RAVE
    • Strong Programming skill set
    • Knowledge of Python, building dashboards
    • Knowledge of API programming
    • Demonstrate excellent problem-solving skills, a proactive approach and the ability to make sound decisions
    • Demonstrated skill in leading teams, by example and mentoring staff
    • Excellent oral and written communication and presentation skills
    • Knowledge of clinical trial process and data management, CRF/eCRF Design, CDISC.
    Working knowledge of the relationship and regulatory obligation of the CRO industry with pharmaceutical / biotechnological companies


    • Demonstrated ability to work in a team environment
    • Demonstrated ability to handle multiple competing priorities
    • Proven interpersonal skills
    Responsibilities


    Senior Rave Programmer Responsible for designing the eCRF in leading EDC systems in Rave


    Technical expertise, technical writing ability, and proficiency in

    Systems Development LifeCycle (SDLC) principles.


    Provide technical

    support and troubleshooting for Rave study development as well as site management and user access within supported RAVE modules


    Serve as system administrator to grant user access using iMedidata Cloud Administration for


    RAVE EDC, Coder, Lab Admin, RTSM and MMI (Imaging) provide Oversight, guidance, and design of study build activities on Rave URL.


    Create Advanced Analytics dashboards


    Insights into creating actionable dashboards and deep understanding and knowledge of good interpretation of clinical data


    Responsible for the preparation and /or review draft and final eCRF, edit check specifications for assigned projects to ensure quality and consistency


    Responsible for conducting Quality Control of study design for assigned projects and participate in the validation of EDC studies


    Responsible for the creation and maintenance of library objects within the Global Libraries


    Responsible for ensuring compliance of standard objects usage throughout the business


    Responsible for the management of standard objects within the Global Libraries


    Perform all activities related to specification development for study build and design of databases according to Standard procedures


    Responsible for the review and approval of derivations and edit checks requested by the project teams


    Participate in the development of global, harmonized SOPs and specific quality work instruction for technical service group activities


    Complete work according to *** SOPs, Work Instructions and project specific guidelines in accordance with Good Clinical Practice
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