Clinical Data Systems Design Lead

Allergan

Irvine (CA)

On-site

USD 120,000 - 160,000

Full time

5 days ago
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Job summary

AbbVie Data Science in Irvine seeks a seasoned professional to drive standardization and delivery of clinical data systems. You will design and implement EDC-based solutions, ensuring compliance with CDASH/SDTM and regulatory guidelines.

With 5+ years in EDC environments, you will mentor teams, influence stakeholders, and coordinate across study teams to ensure on-time delivery and data integrity. This role offers opportunities to shape global data standards and drive process improvements.

Qualifications

  • Bachelor’s degree in business, MIS, CS, life sciences or equivalent; Masters preferred.
  • 5+ years of hands-on technical Study build in EDC; Medidata RAVE experience required; Veeva EDC a plus.
  • Deep knowledge of clinical trial processes.
  • Strong CDASH and SDTM knowledge.
  • Proven ability to influence others and coach in a matrixed environment.
  • Excellent communication and analytical skills.

Responsibilities

  • Develop common data standards and ensure designs comply with standards and protocol requirements.
  • Design and develop clinical trial systems with optimal functionality and data flow.
  • Maintain TA- and program-level consistency across design work.
  • Deliver on-time design and delivery of new clinical systems and integrations.
  • Collaborate with CDO and cross-functional teams to align objectives.

Skills

Clinical trial knowledge
Influence without authority
Mentoring/coaching
Communication skills
Analytical skills

Education

Bachelor’s degree or equivalent
Master's degree preferred

Tools

Medidata RAVE
Veeva EDC

Job description

AbbVie Data Science in Irvine seeks a seasoned professional to drive standardization and delivery of clinical data systems. You will design and implement EDC-based solutions, ensuring compliance with CDASH/SDTM and regulatory guidelines.

With 5+ years in EDC environments, you will mentor teams, influence stakeholders, and coordinate across study teams to ensure on-time delivery and data integrity. This role offers opportunities to shape global data standards and drive process improvements.

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