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About AbbVie

AbbVie’s mission is to discover and deliver innovative medicines that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people’s lives across several key therapeutic areas: immunology, oncology, neuroscience, eye care, virology, women’s health and gastroenterology, in addition to products and services across its Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at Follow @abbvie on Twitter, Facebook, Instagram, YouTube and LinkedIn.

Analyst, Warehouse Data (remote flexibility)

Primary North Chicago, Illinois Secondary Req ID 2212719 Category Information Technology Division AbbVie

Purpose :

Describes the primary goals,objective or function or outputs of this position.

AbbVie Data Science is the best-in-class team within its cross-industry peer group and is responsible for

bringing people, process, and technology together to generate business value from clinical trials data. Our

operational model is exemplified through execution and innovation. This role is key to ensuring successful

delivery against the program- and study-level accountabilities assigned to Data and Statistical Sciences.

Responsibilities :

List up to 10 main responsibilities for the job. Include information about the accountability and scope.

Supports data reporting, analysis and regulatory submissions by aggregating clinical trial data from multiple

sources to a centralized data warehouses, and for transforming those data to industry standard formats (e.g.,

SDTM, reporting). Effectively utilizes advanced technology to execute assigned activities

Ensures that the requirements of each study protocol are reflected in the aggregation of data, in the

conformance of data, in the data quality checks, and the use of common data standards. Ensures that

Therapeutic Area (TA)- and program-level consistency is achieved

Accountable for the on-time design and delivery of fit-for-purpose datasets. Utilizes project management

tools to track study progress and plan work. Anticipates and identifies issues that could affect timelines or

quality and develops options and solutions

Interacts with and influences DSS and cross-functional team members to achieve study objectives. Ensures

that assigned work product is synchronized with upstream and downstream dependencies

Ensures adherence to federal regulations and applicable local regulations, Good Clinical Practices (GCPs),

ICH Guidelines, AbbVie Standard Operating Procedures (SOPs), and to functional quality standards. Stays

abreast of new and/or evolving local regulations, guidelines and policies related to clinical development

Responsible for coaching and mentoring Data Science Associates

Participates in DSS and cross-functional innovation and process improvement initiatives

  • Qualifications :

    List required and preferred qualifications up to 10).

     Include education, skills and experience.

    Bachelor’s degree in business, management information systems, computer science, life sciences or equivalent. Masters preferred

    Must have 3+ years of clinical technology experience (e.g., EDC, IRT, ePRO) or 5+ years of experience in a similar technical role. Experience with common industry design and development tools preferred

    Demonstrated understanding of clinical trial process

    Demonstrated SAS and/or SQL programming skills and knowledge of database concepts

    Knowledge of CDASH and SDTM Demonstrated ability to influence of others without direct authority

    Demonstrated effective communication skills

    Demonstrated effective analytical skills

Significant Work Activities: N/A
Travel: No
Job Type: Experienced
Schedule: Full-time

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