System Design Analyst II

AbbVie

Confirmed live yesterday High trust

Hybrid

Quick summary

Work type: Hybrid
Location: Irvine, CA
Salary: $84,500–$162,000 / yr
Posted: 49 days ago
Freshness: Confirmed live yesterday
Closes: Jul 24, 2126
Nearby: 99+ roles within 25 mi

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

Role Posting Log in to save

The System Design Analyst II - HYBRID joins the AbbVie Data Science team to ensure successful delivery of program and study-level accountabilities within the Clinical Data Strategy Organization. This role involves developing common data standards, establishing methodologies for clinical trial systems, and ensuring designs optimize functionality and data flow. The individual is responsible for the on-time design and delivery of new clinical systems, integrations between systems, and necessary modifications to EDC, IRT, and ePRO platforms. Key technical requirements include five years of experience in EDC study builds, specifically with Medidata RAVE, along with knowledge of Veeva EDC. Candidates must possess in-depth expertise in CDASH and SDTM standards while navigating clinical trial processes. The role requires coordinating across cross-functional teams to solve complex data integration problems while adhering to GCPs and ICH Guidelines.

Skills

EDC Medidata RAVE Veeva EDC CDASH SDTM IRT ePRO System Design Project Management Clinical Trial Systems Data Standards ICH Guidelines

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 to identify and resolve risks to timelines or quality.
Ensure all designs achieve consistency across therapeutic areas and programs.
Maintain 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 within 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 in EDC.
Experience with technical study build in Medidata RAVE is required.
In-depth knowledge of clinical trial processes.
In-depth knowledge of CDASH and SDTM.
Demonstrated ability to influence others without direct authority and coach or mentor in a matrixed environment.
Strong communication and analytical skills.

Save