Sr CRA I/II - FSP - Germany

Job description

Join our team as a Senior Clinical Research Associate and play a pivotal role in advancing clinical trials for leading pharmaceutical and biotech companies. Utilize your expertise in clinical monitoring, ICH GCP compliance, and risk-based monitoring to ensure data integrity and regulatory adherence. Grow your career in a dynamic, innovative environment with global impact. Work Schedule. Standard (Mon-Fri). Environmental Conditions. Office. Job Description. Join Us as a Senior Clinical Research Associate (Level I) – Make an Impact at the Forefront of Innovation. We h... Work Schedule. Standard (Mon-Fri). Environmental Conditions. Office. Job Description. Join Us as a Senior Clinical Research Associate (Level I) – Make an Impact at the Forefront of Innovation. We have... clinical monitoring, ich gcp compliance, risk based monitoring, root cause analysis, clinical trial management system,

medical terminology, regulatory compliance, investigator site initiation, clinical trial close out, investigator payment process, report writing, stakeholder management, presentation skills