Analyst, Data Systems

Role: Clinical Data Management Specialist supporting AbbVie's clinical research trials, ensuring data quality, compliance, and system integrity. Responsibilities: review protocols, design and validate data collection systems aligned with study protocols and regulatory standards; oversee data transmission and system performance metrics; mentor research staff on data management, GCP, and GCDMP; assist in process improvements. Requirements: Bachelor’s Degree; 3+ years in clinical research and data systems; 1-2 years supervisory experience; working knowledge of pharmaceutical R&D, GxP, SOPs; experience with electronic source systems preferred. HighValue: clinical research (likely in immunology, oncology, neuroscience), data management systems, GxP compliance, GCDMP, GCP, validation, process improvement, mentorship. WorkSetup: not specified; requires ability to work independently and collaboratively, ensuring high-quality data collection for regulatory submissions.