Strategic Data Lead for Clinical Trials

AbbVie

Irvine (CA)

Hybrid

USD 109,500 - 208,500

Full time

14 days+

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Job summary

AbbVie in Irvine, CA is seeking a Data Strategy Lead for the CDSO. You will own data-related start-up deliverables from protocol development through system go-live, coordinating with cross-functional teams to embed data standards, CRFs and surveillance into clinical plans.

This role requires strong project management, risk oversight, and the ability to translate complex data concepts into actionable decisions for the study team.

Qualifications

  • Bachelor’s degree in business, MIS, computer science, life sciences or equivalent; Master’s preferred; PMP or Lean Six Sigma Green Belt desired.
  • 6+ years pharma/clinical research/data management or 8+ years project management experience.
  • Deep understanding of clinical trial processes and clinical technology.
  • Demonstrated functional leadership and ability to influence without authority.
  • Proven coaching/mentoring ability in a matrix environment.
  • Strong communication and analytical skills.

Responsibilities

  • Own data-related start-up deliverables from protocol development through system go-live.
  • Lead data management start-up end-to-end with cross-functional teams.
  • Ensure data strategy, standards, CRFs and surveillance across studies.
  • Translate data/tech concepts into clear, decision-ready guidance.
  • Drive process improvements and innovations within CDSO.
  • Coach and mentor team members; collaborate across functions.

Skills

Data strategy
Cross-functional leadership
Project management
Clinical data
Analytical skills

Education

Bachelor's degree in business, MIS, CS, life sciences or equivalent
Master’s preferred
PMP or Lean Six Sigma Green Belt desired

Job description

AbbVie in Irvine, CA is seeking a Data Strategy Lead for the CDSO. You will own data-related start-up deliverables from protocol development through system go-live, coordinating with cross-functional teams to embed data standards, CRFs and surveillance into clinical plans.

This role requires strong project management, risk oversight, and the ability to translate complex data concepts into actionable decisions for the study team.

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