Senior Associate, Clinical Pharmacology Scientific Support & Reporting Writing

Role: Scientific writer and data analyst supporting clinical trial documentation and reporting in pharma. Responsibilities: prepare scientific reports and presentations, assist in phase 1 clinical study planning and protocol writing, review protocols, analyze clinical data with software, ensure scientific integrity, integrate data across studies, perform literature searches, participate in process improvements, mentor team members. Requirements: Bachelor's/Master's in Science, 7+ years in pharma or related industry, strong understanding of clinical study principles, proficient in data analysis and report generation, excellent communication skills, experience supporting clinical research and drug development, proven project success. HighValue: focus on clinical trial documentation, data analysis, and protocol development; experience in therapeutic area operations preferred. WorkSetup: not specified; requires ability to independently analyze clinical data and produce high-quality scientific documentation.