Systems Design Analyst II

AbbVie

Hybrid

Quick summary

Work type
Hybrid
Location
Florham, Park
Posted
2 days ago
Closes
Jun 29, 2126

Market check

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

As a Systems Design Analyst II at AbbVie, you will join the Data and Statistical Sciences team in Florham Park, NJ, playing a crucial role in ensuring successful delivery of clinical systems. Your daily responsibilities include developing common data standards, designing and delivering new clinical trial systems, and integrating existing ones while adhering to federal regulations and industry guidelines such as CDASH and SDTM. You will also mentor team members, utilize project management tools to track progress, and lead innovation initiatives. The ideal candidate has a background in business, computer science, or life sciences, with 5+ years of experience in clinical technology roles like EDC, IRT, or ePRO, and proficiency in industry design and development tools.

What you'll do

  • Develops common data standards for clinical trial systems.
  • Designs and benchmarks methodologies for clinical trial system development.
  • Ensures on-time delivery of new clinical systems and integrations.
  • Anticipates and resolves issues affecting project timelines and quality.
  • Leads innovation and process improvement initiatives in DSS and cross-functional teams.
  • Coaches and mentors team members to enhance their skills.

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
  • Strong project management skills with use of industry tools
  • Expertise in clinical trial processes and regulatory compliance (GCPs, ICH)
  • Demonstrated leadership in innovation and process improvement initiatives

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