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  • Posted: Aug 10, 2022
    Deadline: Not specified
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    We offer a full range of consulting, clinical development and commercialisation services from a global network of offices in 46 countries Since our foundation in Dublin, Ireland in 1990, our mission has been to help our clients to accelerate the development of drugs and devices that save lives and improve quality of life. We are a global provider of co...
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    Statistical Programmer II

    The role:

    As a Sr Statistical Programmer II you will be responsible for statistical aspects of clinical and preclinical research projects. Project responsibilities include study design, case report form development, analysis planning and scheduling, analysis and interpretation of data, and reporting of results. May be required to coordinate analysis efforts across multiple research projects conducted for a client.

    You will have strong demonstrable experience in:

    • Programs statistical analyses using an appropriate statistical analysis software tool
    • Ensures the accuracy and consistency of data flow from case report forms to specifications for analysis datasets.
    • Performs quality review of analysis dataset and TFL programs developed by other programmers and biostatisticians.
    • Verifies that tabulation and statistical analysis system programs and associated documentation are archived prior to the creation of final output.
    • Develops new processes and ensures all process improvements are implemented.
    • Takes a lead role in the review of statistical analyses plans and provides essential feedback.
    • Collaborates with other team members to develop quality reports, publications and regulatory submissions.
    • Maintains libraries of documented and validated programs, macros, and procedures which can be reused to aid in department efficiency.
    • Serves as the chief mentor to other programmers.
    • Contributes to departmental initiatives and acts as an SME on technical subjects as applicable.

    We are looking for:

    • Bachelor's degree in a quantitative or scientific field required. Master's preferred.
    • Ideally, 3 years+ of statistical programming experience.
    • Expert knowledge and understanding of analysis data structure standards (ADaM) and a good understanding of conversion data structure standards (SDTM).
    • Expertise in computer programming, statistical analysis systems (SAS), and other procedural languages.
    • Fully understands biometrics procedures, workflows, and software systems.
    • Excellent written and oral communication skills required.

    go to method of application »

    Principal Statistical Programmer

    The Role:

    The Principal Statistical Programmer will be aligned to a project leadership or technical expertise role, encompassing the following responsibilities

    • The Principal Statistical Programmer will be aligned to a project leadership or technical expertise role, encompassing the following responsibilities:-
    • Lead and execute programming deliverables on multiple projects in parallel and ensure that competing priorities are managed appropriately.
    • Lead and manage the assigned programming team's deliverables at the study and program level to ensure project objectives are met within budget, to agreed timelines and to the highest standard of quality.
    • Proactively plan for and implement effective resource planning, task allocation and tracking of workload in accordance with agreed metrics (e.g. KPIs) and quality standards.
    • Serve in a client-facing capacity that demonstrates an ability to anticipate client needs and implement innovative solutions, as appropriate.
    • Develop and foster client relationships through effective project management and communication.
    • Apply exceptional technical capabilities and knowledge of industry trends to develop broad-use technical solutions for the benefit of study teams across the department.
    • Develop, implement and maintain documentation to technically train staff in the appropriate technical solution.
    • Actively participate in the review and approval of programming procedures and techniques.

    Requirements

    • Extensive experience of successfully performing the role of Statistical Programmer,
    • Preferably experience from the clinical research industry.
    • Prior experience of successfully leading multiple projects in parallel or exceptional technical capability, including ability to develop broad-use technical solutions for the department.
    • Bachelor's degree, in a quantitative or scientific discipline, or local equivalent.

    Benefits of Working in ICON:

    Our success depends on the quality of our people. That's why we've made it a priority to build a culture that rewards high performance and nurtures talent.

    We offer very competitive salary packages. And to keep them competitive, we regularly benchmark them against our competitors. Our annual bonuses reflect delivery of performance goals - both ours and yours.
    We also provide a range of health-related benefits to employees and their families and offer competitive retirement plans - and related benefits such as life assurance - so you can save and plan with confidence for the years ahead.
    But beyond the competitive salaries and comprehensive benefits, you'll benefit from an environment where you are encouraged to fulfil your sense of purpose and drive lasting change.

    ICON is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
    If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below.

    go to method of application »

    Senior Clinical System Designer

    Job Overview

    The Senior Clinical System Designer uses technical, industrial, and interpersonal skills to create case report forms (CRFs) for trials.

    • Lead and serve as main point of contact relevant to the Clinical Systems group.
    • Responsible for managing timelines and budget. Directly engages with client and internal cross-functional teams.
    • Organizes, creates, and oversees the administration of training and mentoring for junior levels.
    • Helps prepare materials and participate in industry meetings as a representative of ICON.
    • Assists in the development of materials for the bid defense process and client demonstrations.
    • Creates and maintains libraries for use in designing, developing, and testing all system components for a trial.
    • Provides support and review for the re-use of library items.

    Qualification

    • Bachelor's degree in a technological or clinical field required.
    • Minimum of 7 years of clinical design experience required.
    • Experience with integrations with IXRS desired.
    • Prior CRO experience required.
    • Must have prior experience building from the protocol. Must be able to read and understand protocol, and develop new CRFs with minimal support.
    • Must be comfortable interfacing directly with clients and internal cross-functional teams (Lead Data Managers, Developers).

    Method of Application

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