Sr. Clinical Research Associate

Role: Senior Clinical Research Associate (Sr. CRA) responsible for independently managing clinical trials in a small to medium scope or supporting larger studies under supervision. Objectives include ensuring trial compliance, quality data collection, and adherence to GCP/SOP standards. Responsibilities encompass site management, vendor oversight, protocol development, study start-up, monitoring, and documentation, with a focus on timelines and budgets. Collaborates with cross-functional teams, vendors, CROs, and sites; reports to Sr. CTM or Associate Director. Qualifications: Bachelor's in a relevant science; minimum 4 years’ experience in clinical trial management or monitoring, with strong knowledge of drug development, ICH/GCP guidelines, and SOP application. Skills in organization, communication, problem-solving, and proficiency in MS Office are essential. Preferred: global trial experience. High-Value: involvement in clinical stages, possibly early to late-phase trials, with a focus on chronic disease indications, supporting operational activities from start-up through closeout. Travel up to 20%. Work setup: hybrid with remote options.