Senior Analyst, Clinical Photography and Imaging - HYBRID

Responsibilities:
- Ensure study protocol requirements are reflected in system designs and that common data standards are used.
- Specify systems to optimize functionality, end-user experience, and data flow.
- Accountable for on-time design and delivery of new clinical systems, system integrations, and required changes (e.g., EDC, IRT). Use project management tools to track progress, anticipate issues affecting timelines/quality, and develop options/solutions.
- Ensure TA- and program-level consistency.
- Interact with and influence DSS and cross-functional team members to achieve program and study objectives; synchronize work products with upstream/downstream dependencies.
- Ensure adherence to federal/local regulations, GCP, ICH guidelines, AbbVie SOPs, and functional quality standards; stay current on evolving local regulations/policies.
- Coach and mentor Data Science Associates.
- Participate in DSS and cross-functional innovation and process improvement initiatives.

Qualifications:
- Bachelor’s degree in business, MIS, computer science, life sciences, or equivalent; Master’s preferred.
- 3+ years clinical technology experience (e.g., EDC, IRT, ePRO) or 5+ years in a similar technical role or clinical development role; experience with common industry design/development tools preferred.
- Demonstrated understanding of clinical trial process.
- Knowledge of CDASH and SDTM.
- Ability to influence others without direct authority; effective communication and analytical skills.