Senior Analyst, Clinical Data Systems

AbbVie

Confirmed live today High trust

Quick summary

Work type
On-site
Location
North Chicago, IL
Salary
$84,500–$162,000 / yr
Posted
1 day ago
Freshness
Confirmed live today
Closes
Nov 4, 2126

Market check

Salary context

Below market

How this pay compares to similar roles

Similar $151k
This role $123k
$73k $196k
below market most similar roles pay here above market

This role pays less than 77% of similar roles. Most pay $125,500–$177,412 — the blue band above. At the midpoint, this role pays about $123k versus about $151k 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 130 open roles on FindRole.

Listed pay typically runs $109,500–$208,500 across 122 roles with salary data.

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At a glance

TL;DR · Senior Analyst, Clinical Data Systems

The Senior Analyst, Clinical Data Systems joins the Data Science team to ensure successful delivery of program and study-level accountabilities for clinical trials. This role involves designing and delivering new clinical systems, managing integrations between systems like EDC and IRT, and ensuring that study protocol requirements are reflected in system designs using common data standards. The successful candidate will utilize project management tools to track progress, identify potential timeline risks, and mentor Data Science Associates. Key technical requirements include experience with clinical technologies such as ePRO, as well as knowledge of CDASH and SDTM standards. The position requires navigating complex clinical development processes while maintaining strict adherence to federal regulations, Good Clinical Practices, ICH Guidelines, and internal Standard Operating Procedures to ensure data flow and functional quality.

What you'll do

  • Translate study protocol requirements into system designs using common data standards.
  • Design and deliver new clinical systems, integrations, and modifications to platforms like EDC and IRT.
  • Optimize system specifications for functionality, end-user experience, and data flow.
  • Use project management tools to track study progress and identify potential timeline risks.
  • Ensure all work products comply with federal regulations, GCPs, ICH Guidelines, and SOPs.
  • Coach and mentor Data Science Associates to support team development.
  • Lead innovation and process improvement initiatives across Data Science and cross-functional teams.

What we're looking for

  • Bachelor’s degree in business, management information systems, computer science, life sciences, or equivalent.
  • Master’s degree (preferred).
  • 3+ years of clinical technology experience (e.g., EDC, IRT, ePRO).
  • 5+ years of experience in a similar technical role or in a clinical development role.
  • Experience with common industry design and development tools (preferred).
  • Demonstrated understanding of clinical trial processes.
  • Knowledge of CDASH and SDTM.
  • Demonstrated ability to influence others without direct authority, with effective communication and analytical skills.

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