Associate I, Clinical Pharmacology Scientific Support & Reporting

Role: Support clinical trial documentation and data analysis activities within AbbVie's pharmaceutical development teams, primarily focusing on early-phase (Phase 1) studies. Responsibilities: prepare scientific reports and presentations, assist in constructing Phase 1 study planning documents, write protocols, and perform literature searches. Analyze clinical data using available software to support blinded and unblinded pharmacokinetic assessments, ensuring compliance with protocols and quality standards. Qualifications: Bachelor's in a science-related field with 2+ years or a Master’s in pharmacology or related discipline; associates degree/RN with 6+ years in pharma considered. Skills include strong communication, report generation, data analysis, and presentation creation. High-Value: Early-phase (Phase 1) clinical studies, pharmacokinetics, protocol writing, scientific reporting, cross-functional collaboration in pharma R&D. Work setup and travel details not specified.