System Design Analyst II, Clinical Systems

AbbVie

Confirmed live today High trust

Hybrid

Quick summary

Work type: Hybrid
Location: Florham Park, NJ
Salary: $84,500–$162,000 / yr
Posted: 3 days ago
Freshness: Confirmed live today
Closes: Sep 18, 2126
Nearby: 99+ roles within 25 mi

Market check

Salary context

Below market

How this pay compares to similar roles

Similar $158k

This role $123k

$71k most similar roles pay here $207k

This role pays less than 74% of similar roles. Most pay $123,250–$193,000 — the shaded band above. At the midpoint, this role pays about $123k versus about $158k 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 354 open roles on FindRole.

Listed pay typically runs $109,500–$208,500 across 321 roles with salary data.

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At a glance

TL;DR · System Design Analyst II, Clinical Systems

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System Design Analyst II-Clinical Systems- HYBRID joins the Clinical Data Strategy Organization to ensure successful delivery of program and study level accountabilities. This role involves developing common data standards, establishing methodologies for clinical trial systems, and ensuring designs optimize functionality, user experience, and data flow. The individual is responsible for the on-time design and delivery of new clinical systems, integrations between systems, and required changes to platforms such as EDC, IRT, and ePRO. Key responsibilities include coaching team members, leading innovation initiatives, and ensuring compliance with federal regulations, Good Clinical Practices, and ICH Guidelines. Required expertise includes five years of technical study build in Medidata RAVE, knowledge of CDASH and SDTM standards, and deep understanding of clinical trial processes. The role addresses the challenge of generating business value from clinical trials data through integrated technology and process improvement.

Skills

EDC Medidata RAVE Veeva EDC CDASH SDTM IRT ePRO Clinical Trial Systems Data Standards Project Management Tools Good Clinical Practices (GCP ICH Guidelines

What you'll do

Develop and enforce common data standards for clinical trial systems and protocol requirements.
Establish and maintain methodologies for designing clinical trial systems based on industry standards.
Manage the on-time design, integration, and delivery of new clinical systems like EDC, IRT, and ePRO.
Track study progress using project management tools to identify and resolve risks to timelines or quality.
Ensure all work products comply with federal regulations, Good Clinical Practices (GCPs), and internal SOPs.
Lead cross-functional innovation and process improvement initiatives within the organization.
Coach and mentor team members to support their professional skill development.

What we're looking for

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

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