System Design Analyst II

AbbVie

Confirmed live yesterday High trust
Hybrid

Quick summary

Work type
Hybrid
Location
North Chicago, IL
Salary
$84,500–$162,000 / yr
Posted
49 days ago
Freshness
Confirmed live yesterday
Closes
Jul 24, 2126

Market check

Salary context

Below market

How this pay compares to similar roles

Similar $162k
This role $123k
$71k most similar roles pay here $214k

This role pays less than 75% of similar roles. Most pay $123,512–$200,000 — the shaded band above. At the midpoint, this role pays about $123k versus about $162k for comparable roles.

Based on 240 similar postings.

Employer

About AbbVie

AbbVie is a global biopharmaceutical company focused on discovering and delivering innovative medicines and solutions in immunology, oncology, neuroscience, and eye care. Its products include Humira, Skyrizi, and Rinvoq.

AbbVie currently has 297 open roles on FindRole.

Listed pay typically runs $109,500–$208,500 across 271 roles with salary data.

Most-posted roles

View all roles at AbbVie

At a glance

TL;DR · System Design Analyst II

System Design Analyst II - HYBRID joins the AbbVie Data Science team to ensure successful delivery of clinical trial systems and data strategy initiatives. The role involves developing common data standards, establishing methodologies for designing clinical trial systems, and ensuring designs optimize functionality and user experience. Key responsibilities include managing the on-time design and integration of systems such as EDC, IRT, and ePRO while coordinating with cross-functional teams to meet program objectives. The ideal candidate possesses a degree in business, management information systems, computer science, or life sciences. Required technical skills include five years of experience in EDC study builds, specifically using Medidata RAVE, along with in-depth knowledge of CDASH and SDTM standards. This role addresses the complex challenge of generating business value from clinical trials data while adhering to federal regulations and Good Clinical Practices.

What you'll do

  • Develop common data standards and ensure system designs comply with protocol requirements.
  • Establish and maintain methodologies for designing clinical trial systems based on industry standards.
  • Manage the on-time design and delivery of new clinical systems and integrations like EDC, IRT, and ePRO.
  • Track study progress using project management tools while identifying and resolving risks to timelines or quality.
  • Ensure all designs maintain consistency across therapeutic areas and programs.
  • Ensure compliance with federal regulations, Good Clinical Practices (GCPs), and internal standard operating procedures.
  • Coach and mentor team members to support their professional skill development.
  • Lead cross-functional innovation and process improvement initiatives for the organization.

What we're looking for

  • Bachelor’s degree in business, management information systems, computer science, life sciences, or equivalent.
  • Master's degree is preferred.
  • Must have 5+ years of hands-on technical study build experience in EDC.
  • Experience with Medidata RAVE technical study build is required.
  • In-depth knowledge of clinical trial processes is required.
  • In-depth knowledge of CDASH and SDTM is required.
  • Demonstrated ability to influence others without direct authority and coach or mentor in a matrixed environment.
  • Strong communication and analytical skills are required.

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