Clinical Research Associate (CRA) - Oncology (Remote)

Role: Clinical Site Manager responsible for overseeing site performance and compliance in a country, ensuring adherence to ICH-GCP, local regulations, and company policies across all trial phases. Objectives include developing strong site relationships, managing site activities, and expanding the research territory. Core responsibilities encompass site monitoring, regulatory documentation, issue resolution, collaboration with cross-functional teams, and supporting site qualification and validation. Requirements: Associate's degree or higher with at least 5 years of healthcare experience, including 2+ years in site management/monitoring within biopharma or CRO; fluent in local language and English; strong knowledge of GCP, clinical trial processes, and data management; proficient in IT tools and clinical systems; current driver's license. Preferred skills include experience with oncology or other therapeutic areas, and familiarity with regulatory and pharmacovigilance practices. High-value specifics: role involves extensive domestic/international travel (~65-75%), remote work setup, and working across multiple protocols and therapy areas. The position emphasizes independent judgment, high accountability, and excellent communication and organizational skills.