System Design Analyst II

AbbVie

Confirmed live 2 days ago High trust

Hybrid

Quick summary

Work type: Hybrid
Location: Florham Park, NJ
Salary: $84,500–$162,000 / yr
Posted: 57 days ago
Freshness: Confirmed live 2 days ago
Closes: Jul 16, 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.

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View all roles at AbbVie

At a glance

TL;DR · System Design Analyst II

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System Design Analyst II - HYBRID joins the Data Science team to ensure successful delivery of program and study level accountabilities within the Clinical Data Strategy Organization. The role involves developing common data standards, establishing methodologies for clinical trial systems, and ensuring designs optimize functionality and data flow. Responsibilities include managing the on-time design and integration of clinical systems such as EDC, IRT, and ePRO while leading innovation and process improvement initiatives. The ideal candidate possesses a degree in business, management information systems, computer science, or life sciences. Required technical skills include five years of experience with Medidata RAVE and technical study builds in EDC, along with in-depth knowledge of CDASH and SDTM standards. This role solves complex problems regarding clinical trial data consistency and regulatory compliance within the pharmaceutical research space.

Skills

EDC Medidata RAVE Veeva EDC CDASH SDTM IRT ePRO System Design Project Management Clinical Data Strategy 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.
Use project management tools to track study progress and resolve issues affecting 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.
Veeva EDC technical study build experience is a plus.
In-depth knowledge of clinical trial processes, CDASH (required), and SDTM.
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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