DrugSafety Physician (m/f) We are looking for a Ongoing safety surveillance and signal monitoring Review and assessment of aggregate safety reports Developement and implementation of risk managementprogrammes Provide medical input for periodic reporting documents (PSURs, annual safety reports, ad-hoc reports, etc.) and other clinical regulatory documents ...
Medical Director Oncology (m/f) You are a Licensed Physician? You are a medicalspecialist in Oncology? You would like to work in a dynamic and fast moving company? Then ... you! Apply today for the position as You provide medical expertise in oncology drugdevelopment and benefit & risk evaluation You are responsible for the daily ...
... not signed in. sign in register » View Jobs » Job Details Regulatory Affairs Specialist ref#: SL 1111-20 emp. type: i3 Pharma Resourcing (Con - Full Time updated: 20 ... Resourcing job description: The client is looking for a Regulatory Affairs Specialist to work office based in Berlin. You will have experience in Post Marketing ...
... Management role will be focused specifically in Oncology working within a specialistgroup. A great opportunity for a clinicalprofessional with previous exposure ... i3 Global :: i3 Research i3 Innovus i3 Statprobe i3 Pharma Resourcing i3 DrugSafety...
... to work on complex but fascinating studies that will investigate an Orphan Drug to treat patients suffering from a very rare blood disease. Our client is ... leave. Working within a small but well established clinicalgroup for a very specialist organisation you will be assisting with the development, organisation and ...
... Plasma Germany Home About CSL Behring Products Patient Commitment Quality & Safety CSL Research & Development Clinical Trials Other Areas of Business News Room ... experience within the pharmaceutical industry. A solid understanding of the drugdevelopmentprocess, and specifically, each step within the clinical trial ...
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