24.04.24 | Teilzeit, Vollzeit | Hamburg | AbbVie Deutschland GmbH & Co. KGDisciplines to advance medicines to our patients. This means Statistical planning, design, analysis, and reporting related to clinical studies and other scientific research studies, including review and development of relevant study and project documents Interaction with regulatory agencies Co-ordination
Später ansehen24.04.24 | Teilzeit, Vollzeit | Hamburg | AbbVie Deutschland GmbH & Co. KGDisciplines to advance medicines to our patients. This means Statistical planning, design, analysis, and reporting related to clinical studies and other scientific research studies, including review and development of relevant study and project documents Interaction with regulatory agencies Co-ordination
Später ansehen26.04.24 | Vollzeit | Putzbrunn | W. L. Gore & Associates GmbHGore is a materials science company focused on improving lives through discovery, product innovation and rewarding careers for our Associates. Medical Device Reporting Specialist (f/m/d) - 240710 Putzbrunn near Munich About the Role Calling all champions of safety and superheroes of compliance
Später ansehen26.04.24 | Vollzeit | München | Daiichi Sankyo Europe GmbHProducts - Demonstrates strong scientific expertise within assigned therapeutic area(s) within the franchise - Effectively manages activities and optimize resources and budget to meet business needs; have excellent project management skills - Operational knowledge and experience in prospective
Später ansehen25.04.24 | Vollzeit | Garching bei München | ITM Isotope Technologies Munich SEOutsourcing (f/m/d) - Support clinical outsourcing projects to ensure successful and timely delivery within the budget - Lead cross-functional teams in vendor selection and manage the stakeholders - Prepare request for proposal packages and review proposals for cost comparisons - Negotiate contracts, manage
Später ansehen26.04.24 | Vollzeit | Frankfurt am Main | Merz AestheticsOf regulatory projects, communication with third parties (e.g. consultants, CROs, distribution partner) concerning regulatory issues, management of regulatory consultants - Natural scientific or medical device engineering background (pharmacist, biologist, chemist, etc.) approbation, diploma, master degree
Später ansehen26.04.24 | Vollzeit | Garching bei München | ITM Isotope Technologies Munich SESafety Scientist (f/m/d) - ICSR preliminary assessment and medical review in Argus Safety - Contribute to medical safety relevant sections in Aggregate safety reports and Risk Management Plans - Elaborate and maintain list of safety concerns - Perform signal detection and safety signal assessment - Act
Später ansehen23.04.24 | Vollzeit, Teilzeit | Ludwigshafen am Rhein | AbbVie Deutschland GmbH & Co. KGSafety, and global medical affairs. The Manager works independently in partnership with experts in multiple disciplines to advance medicines to our patients. This means - Statistical planning, design, analysis, and reporting related to clinical studies and other scientific research studies, including
Später ansehen17.04.24 | Vollzeit | München | Daiichi Sankyo Europe GmbHCommunication, and stakeholder scientific engagement. Responsible for managing budgets and resources for the assigned GMA plan activities, in collaboration with Sr Director. - Leads medical readiness activities for market launches and life cycle management for select indications/projects. Gains strategic
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