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Argus Product Manager - Chicago, IL

Job Location: IL - Chicago

Regional Description: Midwest

Job Number: 00515924


- Job description

Argus Product Manager - Chicago, IL   

Job Description:

Accenture LLP seeks an Argus Product Manager in Chicago to lead the implementation and support of applications in support of Drug Safety objectives, including Argus Safety and MedDRA. S/he will perform the following duties: work with the client to understand and manage expectations; lead the implementation of standard and ad hoc reporting process and ensure that the IT team understands the Pharmacovigilance compliance reporting requirements; oversee programming, validation, and generation of reports for data analysis, including periodic reports and ICH PSUR line listings, PBRER (Periodic Benefit-Risk Evaluation Report), DSUR (Drug Safety Update Report), and PADER (Periodic Adverse Drug Experience Report) reports for multiple cases for a single or multiple marketed products, IND (Investigational New Drug Report) and NDA (New Drug Application Report) reports to help scientists analyze the clinical results for drug safety and effectiveness; interpret regulatory changes as they impact technology and provide technology expertise to implement regulatory changes for maintaining compliance; and plan and implement MedDRA version management and upgrades as required by the Director of Drug Safety and Pharmacovigilance Department.

Basic Qualifications:

This position requires at least a bachelor's degree, or its foreign equivalent, in Computer Science, Information Systems/Technology, or Engineering (any), plus 6 years of experience in IT consulting, including the following professional experience: 4 years managing, supporting, and maintaining of ARISg/j, agXchage change files/build development in weblogic server, and Oracle's Argus safety suite; 4 years managing, coordinating, validating, and building servers for the Pharmacovigilance and regulatory applications; 4 years documenting requirements and managing development team for Cognos, including PBRER dataset sheet, clinical and post marketing tabulations, DSUR line listing of serious adverse reactions, and PADER E2B reconciliation reports; 4 years executing regulatory submission of adverse events for post-marketing and investigative drugs through the Argus reporting tool; 2 years utilizing Oracle databases and PLSQL programming to design, develop and manage the adhoc Pharmacovigilance reports.  

Candidates who are interested in this position should click the APPLY button.    

Accenture is an EEO and Affirmative Action Employer of Females/Minorities/Veterans/Individuals with Disabilities   

Equal Employment Opportunity   

All employment decisions shall be made without regard to age, race, creed, color, religion, sex, national origin, ancestry, disability status, veteran status, sexual orientation, gender identity or expression, genetic information, marital status, citizenship status or any other basis as protected by federal, state, or local law.

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