Sie sind hier: Home > Regional > !#platzhalterstadtname!# >

!#platzhalterdienstname!#

Anzeige
Filter

Weitere: Naturwissenschaften und Forschung: 3 Jobs in Baindt

Berufsfeld
  • Weitere: Naturwissenschaften und Forschung
Branche
  • Pharmaindustrie 3
  • Chemie- und Erdölverarbeitende Industrie 1
Berufserfahrung
  • Mit Berufserfahrung 3
  • Ohne Berufserfahrung 2
  • Mit Personalverantwortung 1
Arbeitszeit
  • Vollzeit 3
Anstellungsart
  • Feste Anstellung 3
Weitere: Naturwissenschaften und Forschung

Head of Biobanking

Fr. 24.09.2021
Biberach an der Riß
At Boehringer Ingelheim we develop breakthrough therapies and innovative healthcare solutions in areas of unmet medical need for both humans and animals. As a family owned company, we focus on long-term performance. We believe that, if we have talented and ambitious people who are passionate about innovation, there is no limit to what we can achieve; after all, we started with just 28 people. Now, we are powered by 50,000 employees globally who nurture a diverse, collaborative and inclusive culture.THE POSITIONBoehringer Ingelheim’s biobank has a high impact for the development of innovative medicines by providing a large number of high-quality biospecimens and associated data for future research use. You are responsible to drive, promote and execute the global biobanking strategy with the focus to optimally support our portfolio. You lead a team of biobanking managers responsible for the operational implementation of the strategy. Furthermore, you are well cross-linked within the biobanking community and serve as reliable info-hub for all biobanking related topics. Discover our Biberach site: One of your key responsibilities will be the elaboration on Boehringer Ingelheim's global biobanking strategy in alignment with stakeholders including promotion as well as execution of the strategy. You build and use networks within the biobanking community to monitor advances in biobanking. Moreover, you ensure a functional infrastructure to ensure a high-quality resource of human biospecimens and their longterm availability and usage, be it Boehringer Ingelheim internal or with external providers for biobanking services. You standardize and optimize concepts and processes for biobanking including ethical and compliance aspects. Furthermore, you lead a team of biobanking managers responsible for implementation of the biobanking strategy on an operational level. You will be the main contact person and Info Hub for any biobanking related topic at Boehringer Ingelheim. PhD (e.g. Biology, Biochemistry or similar) with proven working experience in the biobanking field, preferably within the pharmaceutical industry Profound knowledge of and experience in the pharma environment as well as good understanding of clinical biomarker research Personnel management skills with proven track record Proficient communication and negotiating skills to communicate effectively and in an integrative manner with internal and external experts, stakeholders, opinion leaders and CROs/vendors Process-oriented thinking and acting and ability to take decisions Fluent in written and spoken English This is where you can grow, collaborate, innovate and improve lives. We offer challenging work in a respectful and friendly global working environment surrounded by a world of innovation driven mindsets and practices. In addition, learning and development for all employees is key, because your growth is our growth. We also offer a competitive salary, generous amount of vacation time, and numerous benefits towards your wellness & financial health and work-life balance. Plus, an onsite gym (Ingelheim), in-house doctor and best-in-class cafeterias and coffee bars to keep you energized and healthy. Boehringer Ingelheim is an equal opportunity global employer who takes pride in maintaining a diverse and inclusive culture. We embrace diversity of perspectives and strive for an inclusive environment, which benefits our employees, patients and communities. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity or national origin.
Zum Stellenangebot

Studienleiter (m/w/d) Klinische Studien in der Onkologie

Fr. 17.09.2021
Biberach an der Riß
Sie sind auf der Suche nach einer neuen beruflichen Herausforderung? Dann sind Sie bei uns genau richtig. Als Personalexperten unterstützen wir verschiedene Firmen bei der Suche nach passenden Fach-und Führungskräften (m/w/d) und stehen Ihnen als Karriereberater zur Seite. Aktuell suchen wir für unseren namhaften Kunden aus dem Bereich Chemie/Pharma mit Sitz in Biberach an der Riß eine/n: Studienleiter (m/w/d) Klinischen Studien der Phasen I-IV im Therapiegebiet Onkologie Nutzen Sie Ihre Chance und werden Sie Teil dieser Erfolgsgeschichte!In Ihrer neuen Rolle übernehmen Sie die Verantwortung für die globalen Supply Chain Aktivitäten für Investigational Medicinal Products (IMPs) von nationalen und internationalen klinischen Studien der Phasen I-IV im Therapiegebiet OnkologieIn dieser Position fungieren Sie als Hauptansprechpartner für zugewiesene Studien und stellen die rechtzeitige und kosteneffiziente Bereitstellung von klinischem Material sicherSie werden der verantwortliche Leiter des CTSU-Studienteams innerhalb der Matrixstruktur sein, inkl. funktionsübergreifender Zusammenarbeit und Entwicklung von Schnittstellen für alle Supply-Chain-Aktivitäten auf der Basis von geschäftlichen-, regulatorischen- und IndustrieanforderungenDarüber hinaus unterstützen Sie die Untersuchungen als Fachexperte für zugewiesene VerfahrenSie verfügen über einen Masterabschluss in Naturwissenschaften oder ähnlichen Disziplinen, oder alternativ über eine abgeschlossene Berufsausbildung mit Erfahrung in klinischen StudienDarüber hinaus bringen Sie bereits eine mehrjährige Erfahrung in der Versorgung klinischer Studien oder in verwandten Bereichen mit und verfügen über gute GMP/GCP-KenntnisseVorzugsweise konnten Sie außerdem bereits Erfahrung in der Arbeit in einem internationalen Umfeld, sowie in der Teamleitung und im Projektmanagement sammelnFließende Englischkenntnisse in Wort und Schrift, sowie sehr gute Kommunikations-, Verhandlungs-, und Präsentationsfähigkeiten sind unbedingt erforderlichEin sicherer Umgang mit MS Office und die Fähigkeit, sowohl selbstständig als auch im Team zu arbeiten runden Ihr Profil erfolgreich abWir zahlen ein tarifliches Gehalt, das sich an den Tarif der IG Chemie Baden-Württemberg anlehnt, Branchenzuschläge sowie Urlaubs- und Weihnachtsgeld nach den Vorgaben des Bundesverbands für Personaldienstleister (BAP). Mitarbeiter erhalten eine Profi-Ausstattung an Schutz- und Arbeitskleidung und medizinische Vorsorge durch das Werksarztzentrum. Bei uns erhalten Mitarbeiter Prämien zu besonderen Anlässen sowie exklusive Rabatte in über 600 Geschäften und Online-Shops. Zum präventiven Gesundheitsschutz stellen wir Gesundheitsmasken zur Verfügung. Mit der expertum JobApp kommunizieren Mitarbeiter direkt mit dem Ansprechpartner und verwalten das Zeitkonto in der App. Bei Bedarf finanzieren wir individuelle Fortbildungen, die Mitarbeiter langfristig weiterbringen. In Kooperation mit der Allianz und der Nürnberger Versicherung bieten wir eine betriebliche Altersvorsorge. Auch zu anderen ausgeschriebenen Stellen und Karrieremöglichkeiten beraten wir jederzeit gern.
Zum Stellenangebot

Trial Master File (TMF) Specialist

Fr. 17.09.2021
Biberach an der Riß
  At Boehringer Ingelheim we develop breakthrough therapies and innovative healthcare solutions in areas of unmet medical need for both humans and animals. As a family owned company, we focus on long-term performance. We believe that, if we have talented and ambitious people who are passionate about innovation, there is no limit to what we can achieve; after all, we started with just 28 people. Now, we are powered by 50,000 employees globally who nurture a diverse, collaborative and inclusive culture.  THE POSITION We at Boehringer Ingelheim Medicine share one vision: to turn patient-focused innovations into life-changing treatments. We focus on driving medical innovation, combining scientific and patient insights to develop and deliver safe and effective solutions. By concentrating on first-in-class innovations, we aim to set new standards for patient care now and for years to come.   We build on the strongest of all our assets: Our people. We are an agile team with diverse skills, always striving for excellence. We embrace new technologies and trends, make use of broad data and leading analytics. Our professional ethos reflects our personal values. Above all, we are united by our passion for improving healthcare and the enduring commitment to delivering valuable solutions that transform lives today, tomorrow, and beyond. In Clinical Development & Operations, we strive to bring innovation to patients as quickly as possible to improve patient outcomes and quality of life. We focus on delivering treatments to patients faster by accelerating our clinical development whilst striving for constant optimization and refinement. We drive executional excellence and ensure it is at the heart of our strategy, plans and actions. We see the positives in failure and grasp the opportunity to learn, improve and accelerate. We champion agility, encourage the empowerment of our people and endeavor to work more closely with colleagues wherever they are in the organization to enable us to increase the speed of our decision making. We commit to clinical trial site and patient engagement and to generate evidence that will make a difference to patients’ lives. We are looking for a Trial Master File (TMF) Specialist - you contribute to the design, development, implementation, oversight and continuous improvement of Trial Master File (TMF) processes and standards to ensure clinical trial execution excellence. In your role within the Global Documentation Quality Centre in the Clinical Development & Operation department, you are responsible for the overall management of the TMF and to ensure accordance with relevant ICH guidelines, GCP regulatory requirements and other regulations.    For the global end-to end clinical trial documentation process - including all aspects of TMF standards and site collaboration elements - you actively contribute to a consistent approach to the preparation, maintenance, and archive of TMF records. You work in close collaboration with the Trial Documentation Service (TDS) Management, Trial Teams, Business Partners, Service Providers, Inspection teams and other TMF stakeholders to deliver a GCP compliant TMF and to support speed & value. Furthermore, you are committed to service orientated and customer-centric behaviors including visibility to trial teams and to the broader Clinical Development & Operation organization into ongoing work through up-to-date tracking. You maintain high degree of responsiveness to both internal and external requests; drive issue resolution, facilitate tasks and deliverables. You act as a trusted counterpart to the TMF Service Management, global Business and TMF stakeholders for documentation management related topics. This encompasses contribution to processes improvements, learning and change management implementation and support for any TMF contributor to drive acceleration of clinical trials, create value for investigational sites and patients, optimally enable and support clinical trial execution excellence and maximize business efficiency. University degree qualified or comparable professional education, preferably in medicine / science, paramedical science, computer science, business management or related degree First experience in Clinical Development/Operations, business/process consulting, documentation management and/or project management Basic / entry level expertise in process design/management, process consulting and/or project management and/or Clinical Development/Operations Experience in supporting implementation of systems and/or archiving and retrieval systems in the GCP area preferred Demonstrated process engineering/management, project management, documentation management and/or consulting skills Knowledge and understanding on how to develop lean processes and to implement solutions with analytical skills Fluent in written and spoken English This is where you can grow, collaborate, innovate and improve lives. We offer challenging work in a respectful and friendly global working environment surrounded by a world of innovation driven mindsets and practices. In addition, learning and development for all employees is key, because your growth is our growth. We also offer a competitive salary, generous amount of vacation time, and numerous benefits towards your wellness & financial health and work-life balance. Plus, an onsite gym (Ingelheim), in-house doctor and best-in-class cafeterias and coffee bars to keep you energized and healthy. . Boehringer Ingelheim is an equal opportunity global employer who takes pride in maintaining a diverse and inclusive culture. We embrace diversity of perspectives and strive for an inclusive environment, which benefits our employees, patients and communities. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity or national origin.
Zum Stellenangebot


shopping-portal

Hinweis:

Der Internet Explorer wird nicht länger von t-online unterstützt!

Um sicherer und schneller zu surfen, wechseln Sie jetzt auf einen aktuellen Browser.

Wir empfehlen unseren kostenlosen t-online-Browser: