Associate I, Clinical Pharmacology Scientific Support & Reporting

Role: Support early-phase clinical research through scientific reporting, protocol development, and data analysis. Responsibilities: prepare clinical trial reports and presentations, assist in constructing Phase 1 study planning documents, write Phase 1 protocols, and ensure compliance with study procedures and management directives. Requirements: Bachelor's degree in Science or related field with 2+ years of pharmaceutical industry experience, or Master's in pharmacology or related field; strong communication skills; proficiency with software for report generation, data analysis, and presentations. Preferred: experience with literature reviews, competitive intelligence, and pharmacokinetic data analysis, with ability to contribute to process improvements. HighValue: early-phase clinical trials (Phase 1), data analysis, protocol writing, pharmacokinetics, compliance with GxP standards. WorkSetup: not specified.