... development. As a Clinical Research Associate II at ICON, you’ll ... queries Taking responsibility for study cost efficiency Preparation and review of study documentation and feasibility studies for ... medium-sized studies, including study start-up and close-out ...
... world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. ... assigned region during the study start up period Building relationships ... Leading the preparation of study level essential document templates Aiding ...
... documentation, including protocols and clinical study reports Your Profile: Bachelors degree in a scientific or healthcare-related field. Minimum of 2 years of experience as a Clinical Research Associate. In-depth knowledge of ...
... shaping the future of clinical research? Were seeking an experienced Medical ... internal external teams to uphold study protocols and meet the highest standards in scientific and ethical research practices. Key Responsibilities Act as ...
... Site Monitor II (Clinical Research Associate II) with at least ... line with the Study Monitoring Plan (SMP) and will ... Monitoring Responsibilities and Study Conduct Ensuring regulatory, ICH-GCP ... longer active on a study, review and assess training compliance ...
... Helmholtz association. Our mission: Our research seeks to find a balance ... most demanding challenges between basic research and practical application The opportunity ... -motivation, and enthusiasm for innovative research Motivation to work in a ...
... aufbau- und ablauforganisatorischen Maßnahmen des Research LabsMulti-Stakeholder-Management mit anderen Research Labs im I2SN-ForschungsnetzwerkMitwirkung bei ... von Maßnahmen und Aktivitäten im Research Lab (Schaufenster-Vorhaben, Demonstratoren, F& ...
... develop their career in the research and development of cutting-edge ... Communicate and collaborate on global study activities; working closely with the ... the internal project team, Sponsor, study sites, and third-party vendors ...
... Responsible for management of study vendor Manage site quality, including direct supervision of project Clinical Research Associates and monitoring deliverables Qualifications ... full-service clinical contract research organization (CRO). We provide Phase ...
... develop their career in the research and development of cutting-edge ... the internal project team, Sponsor, study sites, and third-party vendors ... Provide oversight and management of study supplies Create and maintain project ...