Senior Manager, RWE Analytics

AbbVie • Mettawa, IL

12h

About The Position

AbbVie's mission is to discover and deliver innovative medicines and solutions 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, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on X , Facebook , Instagram , YouTube , LinkedIn and Tik Tok . Key Responsibilities Apply real-world evidence study design, statistical theories, & technical programming skills to analyze clinical, survey, claims & electronic medical record databases. Serve as the point of contact for the assigned therapeutical area (TA) or product/ indications to manage analytical activities on multiple assigned projects/ studies focusing on RWE analyses from large databases (e.g., medical claims, EMR/EHR, registries) across various therapeutic areas. Responsible for analytical components of reports describing studies, outcomes, & method used & provide specifications to the HEOR researchers. Support clinical trial PRO (patient-reported outcome) endpoint strategies by executing statistical analysis plans & providing consultations to design needed. Interact with HEOR TA scientists & other relevant stakeholders regarding studies design & execution & with other members of the RWE analytics team or other external stakeholders CRO’s to perform QC activities on their studies.

Requirements

• Must possess a Master’s degree in Statistics, Health Economics & Outcome Research, Epidemiology, Health Service Research, or Analytics, or closely related field & 2 years of work experience in data analytics.
• Of experience required, must have 2 years’ experience analyzing data using & demonstrating deep competency with SAS and SAS SQL programming.
• Of experience required, must have 6 months experience: performing data management/analysis using clinical trial data; designing and conducting real-world observational study analysis (claims, surveys, & EMR analyses) & disseminating the results; conducting RWE analysis by using Instant Health Data (IHD) system; & analyzing real-world data to generate RWE with at least 2 of the following databases (MarketScan, OPTUM, OM1, Symphony, & JMDC).
• In a work or academic setting, must have performed 2 projects utilizing advanced statistical modeling.

Responsibilities

• Apply real-world evidence study design, statistical theories, & technical programming skills to analyze clinical, survey, claims & electronic medical record databases.
• Serve as the point of contact for the assigned therapeutical area (TA) or product/ indications to manage analytical activities on multiple assigned projects/ studies focusing on RWE analyses from large databases (e.g., medical claims, EMR/EHR, registries) across various therapeutic areas.
• Responsible for analytical components of reports describing studies, outcomes, & method used & provide specifications to the HEOR researchers.
• Support clinical trial PRO (patient-reported outcome) endpoint strategies by executing statistical analysis plans & providing consultations to design needed.
• Interact with HEOR TA scientists & other relevant stakeholders regarding studies design & execution & with other members of the RWE analytics team or other external stakeholders CRO’s to perform QC activities on their studies.

Benefits

• We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.
• This job is eligible to participate in our short-term and long-term incentive programs.

What This Job Offers

• Job Type: Full-time
• Career Level: Senior