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      • Biberach Baden, Baden-Württemberg
      • Arbeitnehmerüberlassung
      • €50.000 - €55.000 pro Jahr
      • Randstad Deutschland
      Have you just completed your apprenticeship as a Clinical Trial Administrator or would you like to reinvent yourself professionally? We can help you! We are currently looking for a Pharmacist at our location in Biberach. Your passion for team work and your ability to learn quickly are the keys to an exciting new career!Das dürfen Sie erwartenAttractive pay accoring to the BAP/DGB collective agreementReliable and punctual payments, possibility of monthly installments on accountExtensive social benefits, incl. Christmas and holiday bonusesFree personal protective equipmentIhre AufgabenSupport of planning, managing and steering of timelines, costs and scope of Trial Teams for agreed deliverables of global supply chain activities for assigned clinical trials, including highly complex trials (e.g. Mega trials, adaptive trial design, digital trials, trials fully outsourced to a third party (CRO)) and Investigator Initiated Studies (IIS), EAP as well as NPU programs)Responsible to support Trial Managers for the autonomous management of the CTSU trial team within the matrix structureSupport of CTS preparation documentationSupport of team meetings, minutes with action points and responsibilitiesSupport of different systems like BIRDS (BI System) administration and workflows, Focus entries/updates, CES entries/updates, AC Evaluation coordination, AC Ordering, MLT drafting prior to TrM review/approval, GTL maintenance, manuel release form as well as manuel shipping request for bulk shipments, stability samples and sampling documentation for Investigational Medicinal ProductsUnsere AnforderungenBachelor's-Degree with some years of relevant experienceRelevant experience in Pharmaceutical industryBasic project management skillsBroad and thorough knowledge and understanding of applicable US and EU regulations and other international regulationsDemonstrate strong problem solving capabilities and encourage the implementation of innovative approaches, new technologies and strategies to support the successful completion of supply chain activitiesProven ability to drive results in a changing environment and to discuss and present proposals in a concise and effective mannerExcellent written and verbal communication skillsDemonstrated ability to present projects/status reports to different audiencesVery good to fluent in English, spoken and writtenWillingness to travelStrong computer skills (e.g. Microsoft Office 365, Project Management Software) Corona virus & applying at GULP: The health of our candidates and employees as well as our social responsibility are our highest priority. In addition to working conditions that take into account all currently necessary precautionary measures, our application process is also possible without direct and personal contact.
      Have you just completed your apprenticeship as a Clinical Trial Administrator or would you like to reinvent yourself professionally? We can help you! We are currently looking for a Pharmacist at our location in Biberach. Your passion for team work and your ability to learn quickly are the keys to an exciting new career!Das dürfen Sie erwartenAttractive pay accoring to the BAP/DGB collective agreementReliable and punctual payments, possibility of monthly installments on accountExtensive social benefits, incl. Christmas and holiday bonusesFree personal protective equipmentIhre AufgabenSupport of planning, managing and steering of timelines, costs and scope of Trial Teams for agreed deliverables of global supply chain activities for assigned clinical trials, including highly complex trials (e.g. Mega trials, adaptive trial design, digital trials, trials fully outsourced to a third party (CRO)) and Investigator Initiated Studies (IIS), EAP as well as NPU programs)Responsible to support Trial Managers for the autonomous management of the CTSU trial team within the matrix structureSupport of CTS preparation documentationSupport of team meetings, minutes with action points and responsibilitiesSupport of different systems like BIRDS (BI System) administration and workflows, Focus entries/updates, CES entries/updates, AC Evaluation coordination, AC Ordering, MLT drafting prior to TrM review/approval, GTL maintenance, manuel release form as well as manuel shipping request for bulk shipments, stability samples and sampling documentation for Investigational Medicinal ProductsUnsere AnforderungenBachelor's-Degree with some years of relevant experienceRelevant experience in Pharmaceutical industryBasic project management skillsBroad and thorough knowledge and understanding of applicable US and EU regulations and other international regulationsDemonstrate strong problem solving capabilities and encourage the implementation of innovative approaches, new technologies and strategies to support the successful completion of supply chain activitiesProven ability to drive results in a changing environment and to discuss and present proposals in a concise and effective mannerExcellent written and verbal communication skillsDemonstrated ability to present projects/status reports to different audiencesVery good to fluent in English, spoken and writtenWillingness to travelStrong computer skills (e.g. Microsoft Office 365, Project Management Software) Corona virus & applying at GULP: The health of our candidates and employees as well as our social responsibility are our highest priority. In addition to working conditions that take into account all currently necessary precautionary measures, our application process is also possible without direct and personal contact.

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