Associate, Data Sciences II

Role: Data Science professional supporting clinical trial data management and analysis within AbbVie's clinical development. Responsibilities: execute study assignments aligned with trial concepts and protocol requirements; engage with cross-functional teams, utilize data standards (CDASH, SDTM) for data flow and system interfaces; support study start-up, conduct, and close-out processes; perform data analyses for operational decision-making; develop clinical trial application design specs; ensure compliance with GCP, ICH, and local regulations. Requirements: Bachelor's in life sciences, computer science, or related field; 2+ years in clinical research, analytics, or a similar area; strong communication, problem-solving, and project management skills; ability to work effectively in fast-paced environments. Preferred: Master’s degree; experience with clinical trial systems and data standards. High-Value: focus on clinical trial data management and analytics in a biopharma setting, with an emphasis on regulatory compliance, GCP adherence, and cross-functional collaboration. Work setup: not specified, likely hybrid or office-based based on typical roles.