Clinical Research Associate I (CRA I) / Klinischer Monitor – Full-Time or Part-Time Available (m/w/d)

Job description

We are expanding our team: As a Clinical Research Associate I, you will monitor clinical trial sites, ensure protocol and regulatory compliance, and support data accuracy. Ideal candidates have experience in clinical research and strong monitoring skills. Work Schedule. Standard (Mon-Fri). Environmental Conditions. Office. Job Description. At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Jo... Work Schedule. Standard (Mon-Fri). Environmental Conditions. Office. Job Description. At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join... clinical monitoring, ich-gcp compliance, risk based monitoring, site management, sdr, sdv, crf review, clinical trial management system, regulatory documentation, root cause analysis, medical terminology, clinical research, investigator

site initiation, audit readiness, investigational product assessment, trial close out, file review, business writing, critical thinking, problem solving, team collaboration, presentation skills, organizational skills, time management, process improvement