... to shape the future of clinical development. As a Clinical Research Associate II at ICON, you’ll work within a large-scale, fast-paced environment alongside a close-knit team of highly qualified CRAs to identify, select, initiate and ...
... , including direct supervision of project Clinical Research Associates and monitoring deliverables Qualifications Bachelor’s ...
... , Germany Bielefeld, North Rhine-Westphalia, Germany Bremen, Bremen, Germany Leipzig, Saxony, Germany Nurnberg, Bavaria, Germany Saarbrucken, Saarland, Germany Erfurt, Thuringia, Germany Kiel, Schleswig-Holstein, Germany Osnabruck, Lower Saxony, Germany ...
... , training and work experience in clinical trials At least 3 years of experience as a Clinical Project Manager (CPM) or 5-6 years as Clinical Research Associate (CRA) at a CRO medical device ...
... are knowledgeable about treatment guidelines, clinical research processes, and EU pharma regulations ...
... are knowledgeable about treatment guidelines, clinical research processes, and EU pharma regulations ...
... are knowledgeable about treatment guidelines, clinical research processes, and EU pharma regulations ...
... global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development and technology ...
... ensure that medical and clinical activities in Germany are in sync with global ... medical guidance to local clinical research teams. Assessing medical education needs ... Medical Affairs and Clinical Development in Germany. You possess a thorough understanding ...
... Office Based (NRW) As a Clinical Trial Associate you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. ... : tracks progress of the clinical trial, manages study data, budget, ...