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    Technical Product Manager - Phoenix, United States - Imperatrix Datum Solutions Corporation

    Imperatrix Datum Solutions Corporation
    Imperatrix Datum Solutions Corporation Phoenix, United States

    1 week ago

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    Description

    SUMMARY
    Imaging Endpoints (IE) is an Imaging Technology and Imaging Clinical Research Organization (iCRO). We are passionately focused on our vision to Connect Imaging to the Cure TM . Everything we do is aligned with this singular purpose. We work every day excited to advance imaging science, technology, and services to bring curative technologies to humankind.

    We have supported many of the most impactful new drug approvals in oncology, and we are seeking the most talented individuals globally that are passionate in their desire to assist us in our mission to customize each clinical trial's imaging to optimize the opportunity to demonstrate efficacy.


    Imaging Endpoints is based in Scottsdale, Arizona, with offices in Cambridge, Massachusetts; London, UK; Leiden, Netherlands; Basel, Switzerland; Hyderabad, India and Shanghai, China.

    We are an affiliate of HonorHealth, one of the largest healthcare systems nationally, and Scottsdale Medical Imaging Limited (SMIL/RadPartners), the largest private radiology group in the United States.

    We are recognized as the world's largest and most preeminent iCRO in oncology.


    Under the direction of Imaging Operations Leadership this position is primarily responsible for configuring and administrating Imaging Endpoints Clinical Trial Management System (CTMS).

    This role will coordinate with the CTMS vendor and will administrate iCTMS activities related to new CTMS builds, updates to existing CTMS builds, user administration, report development, system enhancements, investigating new scope for automation for system improvements, lay process improvement plans for Imaging Endpoints and general responses to issues experienced by CTMS users.


    RESPONSIBILITIES
    Assist with day-to-day administration of CTMS

    Strong problem-solving skills and ability to work independently

    Provide functional guidance of CTMS application to various stake holders

    Access Management for CTMS application to cross functional department as well as stake holders

    Configure new study builds within CTMS application per study specific requirements and configuration management change control requirements

    Create and configure customized global and project specific reports within CTMS application

    Assist in the creation and maintenance of training materials for CTMS application navigation and functionality

    Coordinate with Compliance and Regulatory Affairs teams in performing necessary activities for study new builds, study build updates

    Assist in the training of internal users on iCTMS

    Other duties as assigned by the manager


    EDUCATION AND EXPERIENCE
    Bachelor's degree or equivalent work experience required

    Minimum of 1-2 years in Healthcare and/or Clinical trials industry preferred

    Sybase, SQL reports, or query writing experience is a must

    Must have strong computer skills

    Proficiency in MS Office and internet applications required

    Knowledge of Good Clinical Practice (GCP), Quality Assurance/Compliance in a clinical trials setting is preferred


    SKILLS
    Service oriented approach, flexible, and proactive

    Must have superior attention to detail and excellent oral and written communication skills

    Self-driven, can-do positive attitude

    Ability to excel in a team environment

    Ability to work in strict compliance with all procedures, rules, and regulations

    Maintain strict confidentiality of sensitive data, records, files, conversations, etc.

    Must be self-motivated and able to grasp new concepts quickly

    Ability to prioritize workload to the changing needs of the day-to-day business

    Ability to understand technical research protocols and successfully lead within the research environment

    Ability to manage project activities with diverse group and individuals with little supervision


    IMAGING ENDPOINTS' TEAM CHARACTERISTICS
    Passion to

    Connect Imaging to the Cure TM

    and pursue a meaningful career by improving the lives of cancer patients through imaging

    Strong desire to be part of a dynamic, global team working closely together and growing year after year in a rewarding environment to help humanity through imaging

    Commitment and caring for our fellow team members, their families, and the communities IE serves – see more information about Caring Endpoints at

    Integrity and high ethical standards; we always do the right thing

    High intellect and ingenuity; we enjoy solving problems, finding a better way, and the challenge of making a difference by improving lives

    Structured, organized, detail-oriented, and self-motivated; we approach each day with a detailed plan and excitement to accomplish the day's objectives while striving to improve ourselves and IE everyday

    Accountable; we do what we say and communicative effectively to meet deadlines; we enjoy advancing clinical trials, helping patients, and celebrating success

    High standard for excellence; we proof our own work, hold high standards for ourselves and our team, and always prioritize quality above all else


    PHYSICAL REQUIREMENTS


    While performing the duties of this job, the employee is regularly required to use hands to finger, handle, or feel; reach with hands and arms and talk and hear.

    The employee is frequently required to sit. Specific vision abilities required by this job include close vision, color vision, ability to adjust focus.

    Travel:
    Up to 5% (domestic and/or international)

    #J-18808-Ljbffr
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