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 ansehen27.04.24 | Vollzeit | Marburg | CSL BehringTeams for multiple CSL Behring recombinant projects in either early or late-stage clinical development. The primary responsibility and accountability of the role is to establish and manage the product development strategy and deliver the scientific content for the Quality Section of Health Authority
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 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 ansehen22.04.24 | Vollzeit | Rostock | ZEISSFor advanced microscopy. Our portfolio includes equipment, software and services for life sciences, materials and industrial research as well as for education and clinical practice. ZEISS microscopes are the preferred choice of scientific pioneers and enable leading researchers to find answers to our society's
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