Associate I, Clinical Pharmacology Scientific Support & Reporting

Role: Clinical research assistant supporting phase 1 clinical trial documentation and data analysis within AbbVie's drug development teams. Responsibilities: prepare scientific reports, contribute to phase 1 study planning and protocol writing, analyze clinical trial data including pharmacokinetics, and ensure compliance with study procedures and quality standards. Requirements: Bachelor's in Science or related field with 2+ years in pharma, or Master's in pharmacology or similar; strong communication skills; proficiency in report generation, data analysis, and presentation software. Preferred: experience with clinical study data and process improvement. HighValue: focus on early-phase (Phase 1) clinical trials, data analysis, protocol development, and regulatory compliance in a biopharma setting. WorkSetup: not specified; likely office-based with potential for cross-functional collaboration.