Sr. Clinical Research Associate

Role: Senior Clinical Research Associate (Sr. CRA) responsible for managing clinical trial activities for a small to medium-sized study or supporting large-scale projects. Objectives include ensuring protocol compliance, site management, vendor oversight, and adherence to GCP/ICH standards. Responsibilities encompass study start-up, site management, vendor coordination, trial documentation, and quality assurance activities. The Sr. CRA supports study design input, monitors trial progress, and manages trial-related logistics such as drug supply and regulatory documentation. Qualifications: Bachelor's in a relevant scientific discipline; minimum 4 years' clinical trial management experience, preferably with Sponsor or CRO; strong understanding of drug development, GCP/ICH guidelines, and clinical trial processes. Skills include excellent organizational, communication, problem-solving abilities, proficiency in MS Office, and ability to work independently. Travel up to 20% required. High-value specifics: experience with clinical trials in cardiovascular, metabolic, or pulmonary indications; involvement in early to late-phase studies; global trial experience preferred; familiarity with vendor management, clinical documentation, and trial oversight.