Systems Design Analyst II

AbbVie

Hybrid

Quick summary

Work type: Hybrid
Location: Irvine, CA
Posted: 2 days ago
Closes: Jun 29, 2126
Nearby: 99+ roles within 25 mi

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Salary context

How this pay compares to similar roles

Similar $156k

$107k most similar roles pay here $202k

This listing doesn't post a salary. Most similar roles pay $125,075–$186,900.

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 67 open roles on FindRole.

Listed pay typically runs $109,500–$208,500 across 5 roles with salary data.

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At a glance

TL;DR · Systems Design Analyst II

Role Posting Log in to save

As a Systems Design Analyst II at AbbVie, you will join the Data and Statistical Sciences team in Irvine, CA, playing a crucial role in ensuring successful delivery of clinical systems. Your responsibilities include developing common data standards, designing and implementing clinical trial systems such as EDC, IRT, and ePRO, and maintaining methodology to optimize functionality and user experience. You will also manage project timelines, ensure regulatory compliance, and mentor team members while driving innovation and process improvements across the organization. The ideal candidate has a background in business, computer science, or life sciences with extensive clinical technology experience, proficiency in CDASH and SDTM, and strong analytical and communication skills.

Skills

EDC IRT ePRO CDASH SDTM CI/CD SQL Python R SAS AWS Azure GCP Kubernetes Docker Git JIRA Confluence Terraform PostgreSQL

What you'll do

Develops common data standards for clinical trial systems.
Designs and develops clinical trial systems, ensuring compliance with industry standards.
Ensures on-time delivery of new clinical systems and integrations.
Anticipates issues affecting timelines or quality in project management.
Coaches and mentors team members to enhance skill development.
Leads innovation and process improvement initiatives within the organization.
Ensures adherence to federal regulations and Good Clinical Practices.

What we're looking for

5+ years of clinical technology experience (e.g., EDC, IRT, ePRO)
Bachelor’s degree in relevant field; Master's preferred
In-depth knowledge of CDASH and SDTM standards
Proven ability to coach and mentor team members effectively
Experience with common industry design and development tools
Strong communication and analytical skills required
Ensures compliance with federal regulations, GCPs, ICH Guidelines

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