Sr. Clinical Research Associate

Role: Senior Clinical Research Associate (Sr. CRA) responsible for independently managing all clinical aspects of small to medium-sized studies, and supporting large-scale trials under supervision. Objectives include ensuring compliance with GCP, SOPs, and study protocols, while delivering high-quality data and study execution. Responsibilities: oversee site management, monitor vendor activities, support protocol development and amendments, manage timelines and budgets, and ensure regulatory and document compliance. Qualifications: Bachelor’s degree in a relevant science, 4+ years of clinical trial management experience, strong understanding of drug development, ICH/GCP guidelines, and clinical operations. Skills include proficiency in Microsoft Office, site management, vendor oversight, and excellent communication. Preferred qualifications: global trial experience. High-value specifics: experience with small molecule therapeutics, clinical-stage (likely Phase 1-3), and a focus on cardiovascular, metabolic, or pulmonary indications. Role involves up to 20% travel and reports to a Sr. CTM or Associate Director. Work setup: hybrid, with flexible remote options.