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Stellenangebote für Regulatory Jobs in Großbritannien

Top Job - Basel (Basel-Stadt) - F. Hoffmann-La Roche AG

But not limited to diagnostics product planning and prioritization, new product discovery, reimbursement and regulatory use. The PHS Team Leader is able to act as a subject matter expert as well as a key partner for strategic portfolio planning and execution within DIS. In this position, you will

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Ihre Aufgaben · Fachliche und personelle Führung eines kleinen Teams · Planung und Koordination der Aktivitäten im Bereich Registrierung und Medical · Sicherstellung der Einhaltung von regulatorischen Anforderungen · Unterhalt, Erweiterung und Sicherstellung bestehender Produktzulassungen · Überwac

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Top Job - Zürich - Ernst & Young AG

Out both reactive and proactive data analysis of large volumes of unstructured and structured data. Working with clients, fraud investigators, internal and external auditors, lawyers and regulatory authorities in sensitive and sometimes adversarial situations. Working in our specialist forensic

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20.02.18 - Zürich, Paris, Frankfurt am Ma... - 80.000 - 100.000

To other departments, - Monitoring regulatory developments. Profile - Significant experience as an intern in a law firm or in a legal department, with exposure to Private Equity - Venture Capital, ideally in the UK - Lawyer or Master Degree in Law REMUNERATION MENSUELLE 1823? (indemnité non

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20.02.18 - Zürich - 40.000 - 60.000

Structure - Coordination and approval of client regulatory report requests - Support the Team Head in various strategic and operative Global Sales projects - At least 5-8 years of sales or marketing support or assistant experience, preferably in Asset Management - Strong communication and interpersonal

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20.02.18 - Welwyn Garden City, Basel (Bas... - 150.000 - 200.000

Interactions and communications - Works with regulatory and other internal partners/stakeholders in the completion and submission of regulatory filings and other regulatory documentation. Supports others with clinical science information and input for regulatory submissions and other regulatory processes

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14.02.18 - Welwyn Garden City, Basel (Bas... - 100.000 - 125.000

Position OverviewThe Global Faster Filing Program Management Office is being created in the Global Product Development Regulatory (PDR) organization on behalf of the Roche enterprise. The goal of the Global Faster Filing Office is to enable us to be best in class and get our new medicines to

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14.02.18 - Welwyn Garden City, Basel (Bas... - 80.000 - 100.000

Illnesses. Please take this opportunity to learn about Genentech where we believe that our employees are our most important asset & are dedicated to remaining a great place to work. The Global Faster Filing Program Management Office is being created in the Global Product Development Regulatory (PDR

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06.02.18 - Zug, Cambridge, Brighton - 80.000 - 100.000

Statistical methodology - Provide support to the regulatory submissions - BA/BS degree in statistics, computer science, biostatistics, mathematics or related field. - Minimum five years of Biostatistical experience in a CRO or Pharmaceutical environment experience. - Demonstrated ability to successfully lead

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06.02.18 - Zug, Cambridge, Brighton - 40.000 - 60.000

Serving as Lead Biostatistician on assigned studies, they will contribute to the clinical trial protocols, create the Statistical Analysis Plans, prepare Clinical Study Reports and lead the statistical sections of regulatory agency meetings (FDA, EMA, PMDA, etc.). Longer term, the role has some very

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01.02.18 - Pfäffikon - 60.000 - 80.000

No two days are the same - experience of large regulatory programmes @ UBS highly desirable - Professional Project Management certifications desirable You are - a strong written and verbal communicator, comfortable interacting with colleagues at all levels - an expert at building networks and

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31.01.18 - Basel (Basel-Stadt) - F. Hoffmann-La Roche AG

Approval. You ensure GCP, Clinical Operating Guidelines and Standard Operating Procedures are followed within PDC. You liaise with appropriate departments inside and outside PDC to define the timing of discussion with the FDA and other regulatory bodies on format of clinical NDA and submission issues. You

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31.01.18 - Basel (Basel-Stadt), San Franc... - F. Hoffmann-La Roche AG

Development strategy development and presents to various internal committees Provide clinical oversight across all relevant studies and programs Lead and participate in ongoing CST and relevant sub-team meetings, other interactions and communications Work with regulatory and other internal partners

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IHRE AUFGABEN Überprüfen, Erstellen und Einreichen der Schweizer Zulassungsdossiers Unterhalt und Erweiterung bestehender Produktzulassungen (Lifecycle-Management) Prüfung und Freigabe von Verpackungen, Produktetiketten und Arzneimittel-informationen Direkte Ansprechperson für die Zulassungsbehörde

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Top Job - Zürich

Regulatory Reporting Specialist (ZUR00023) Job Description Regulatory Reporting Specialist-ZUR00023 As a global investment manager, we help institutions, intermediaries and individuals across the planet meet their goals, fulfil their ambitions, and prepare for the future. But as the world changes

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