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AbbVie

System Design Analyst I, Clinical Data Systems

AbbVie

. Design and deliver new clinical systems and integrations, including EDC and IRT, and implement required system changes .

Posted 10/7/2026full-timeRemote • California • United StatesMid-LevelSenior💰 $78,500 - $141,000 per yearWebsite

Core Competencies

Role fit
Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in designing and delivering clinical systems and integrations, ensuring compliance with federal regulations and industry standards. Proficient in project management and optimizing systems for functionality and user experience.

Highest-signal resume keywords
Clinical Technology ExperienceEDC System DesignIRT ImplementationKnowledge of CDASH and SDTMEffective Communication Skills

ATS Keywords

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Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills
Clinical Systems DesignProject ManagementData Flow OptimizationRisk Identification and MitigationSystem Integration
Soft Skills
Coaching and MentoringInfluencing Without AuthorityAnalytical Skills
Tools & Technologies
Project Management ToolsEDCIRTEPRO
Industry Keywords
GCPICH GuidelinesSOPsClinical Trial ProcessCommon Data Standards

About the role

Key responsibilities & impact
  • Design and deliver new clinical systems and integrations, including EDC and IRT, and implement required system changes
  • Use project management tools to track study progress and plan work
  • Identify timeline or quality risks and develop solutions
  • Ensure study protocol requirements are reflected in system designs and common data standards are used
  • Optimize systems for functionality, end-user experience, and data flow
  • Ensure therapeutic-area and program-level consistency
  • Collaborate with DSS and cross-functional team members to achieve program and study objectives
  • Synchronize work products with upstream and downstream dependencies
  • Ensure adherence to federal and local regulations, GCPs, ICH Guidelines, SOPs, and functional quality standards
  • Monitor evolving regulations, guidelines, and policies related to clinical development
  • Coach and mentor Data Science Associates
  • Participate in DSS and cross-functional innovation and process-improvement initiatives

Requirements

What you’ll need
  • Bachelor's degree in business, management information systems, computer science, life sciences, or equivalent
  • Master's degree preferred
  • 3+ years of clinical technology experience, such as EDC, IRT, or ePRO; or 5+ years of experience in a similar technical or clinical development role
  • Experience with common industry design and development tools preferred
  • Demonstrated understanding of the clinical trial process
  • Knowledge of CDASH and SDTM
  • Ability to influence others without direct authority
  • Effective communication skills
  • Effective analytical skills

Benefits

Comp & perks
  • Paid time off, including vacation, holidays, and sick leave
  • Medical, dental, and vision insurance
  • 401(k)
  • Short-term incentive programs
  • Remote work option
  • Equal opportunity employment
  • Reasonable accommodation for US and Puerto Rico applicants