Clinical Research Associate (CRA) - Immunology-Remote

Role: Country Site Manager responsible for overseeing clinical trial site performance and compliance across designated regions (Texas, Illinois, Arizona, Florida, California, NY, Colorado). Objectives: ensure adherence to ICH-GCP, local regulations, and company policies; develop and maintain strong site relationships; expand site network; and support trial conduct. Responsibilities include monitoring site activities, managing regulatory documentation, coordinating with cross-functional teams (regulatory, pharmacovigilance, legal), and participating in site selection and validation. Travel up to 75% domestically and internationally; current driver’s license required. Qualifications: at least 5 years in healthcare or clinical research, with 2+ years of direct site management or monitoring experience; Associate’s or Bachelor’s degree in a scientific or healthcare discipline; fluency in English and local language; strong understanding of GCP, clinical trial phases, and regulatory standards; proficient in clinical IT tools and documentation practices. Skills include site management, data review, problem resolution, and effective communication. Behavioral traits emphasize independence, organization, cultural sensitivity, and high compliance standards. High-value specifics: focus on clinical trial execution, site development, and monitoring in a regulated environment; extensive travel; remote work flexibility; and experience managing multiple protocols across diverse regions.