shape the future of clinical development. What you will be doing: As a Clinical Research Associate at ICON, you’ll work within a large-scale, fast-paced environment alongside a close-knit team of highly qualified CRAs to

Position : Senior Clinical Research Associate Germany - Sponsor Dedicated Erfahrung : 1-3 Jahre als Senior Clinical Research Associate Ort : Deutschland (remote) Sind Sie sich sicher, dass Sie auch wirklich den Job

einen Clinical Research Associate (CRA)/Senior CRA/Klinischen Monitor (m/w/d) • Planung, Vorbereitung und Durchführung von Monitoringvisiten gemäß SOPs (sowohl onsite als auch remote) • Fristgerechte Erstellung von Berichten

development options. Competitive salary package (up to around 80.000€ p.a.) according to your experience level. Ideal for experienced Clinical Research Associate who is looking for a better career development and new challenges

development options. Competitive salary package (up to around 80.000€ p.a.) according to your experience level. Ideal for experienced Clinical Research Associate who is looking for a better career development and new challenges

development options. Competitive salary package according to your experience level. Ideal for experienced Clinical Research Associate who is looking for a better career development and new challenges, great chance to develop

development options. Competitive salary package according to your experience level. Ideal for experienced Clinical Research Associate who is looking for a better career development and new challenges, great chance to develop

als CRA Beherrschung der englischen und deutschen Sprache Kenntnisse der EU-Vorschriften für klinische Forschung und ICH-GCP Gute Präsentations- und Kommunikationsfähigkeiten Sie können mich auch für andere Stellen im Bereich

als CRA Beherrschung der englischen und deutschen Sprache Kenntnisse der EU-Vorschriften für klinische Forschung und ICH-GCP Gute Präsentations- und Kommunikationsfähigkeiten Sie können mich auch für andere Stellen im Bereich

als CRA Beherrschung der englischen und deutschen Sprache Kenntnisse der EU-Vorschriften für klinische Forschung und ICH-GCP Gute Präsentations- und Kommunikationsfähigkeiten Sie können mich auch für andere Stellen im Bereich

experience as a CRA Work proficiency in English and German Knowledge of EU clinical research regulations & ICH-GCP Good presentation and communication skills Who we are and WHY us We are professional global recruitment agency

experience more than 1 year Site management experience as a CRA Work proficiency in English and German Knowledge of EU clinical research regulations & ICH-GCP Good presentation and communication skills Who we are and WHY us We are

experience more than 1 year Site management experience as a CRA Work proficiency in English and German Knowledge of EU clinical research regulations & ICH-GCP Good presentation and communication skills Who we are and WHY us We are

experience more than 1 year Site management experience as a CRA Work proficiency in English and German Knowledge of EU clinical research regulations & ICH-GCP Good presentation and communication skills Who we are and WHY us We are

Naturwissenschaften, Pharmazie, Biotechnologie oder vergleichbar. • Du bringst bereits erste Berufserfahrung (min. 1 Jahr) als Clinical Research Associate (CRA) mit und besitzt ein grundlegendes Verständnis der GCP-Anforderungen

key areas: monitoring and clinical research associate support, R&D study material logistics, and data and document management. Additionally, you will spearhead initiatives to identify efficiencies and enhance processes

Operations Coordinator, Clinical Laboratory Scientist, Biomedical Scientist, Principal Scientist, Laboratory Manager, Clinical Research Scientist, Biotechnology Research Scientist, Pathology Lab Director, Associate Research

Operations Coordinator, Clinical Laboratory Scientist, Biomedical Scientist, Principal Scientist, Laboratory Manager, Clinical Research Scientist, Biotechnology Research Scientist, Pathology Lab Director, Associate Research

. Keeping senior management apprised of the safety profile of designated drugs and suggesting PV/RM actions IHR PROFIL Medical degree with clinical and/or clinical research experience. Proficient knowledge in pharmacovigilance (PV