Stellenangebote für Cross

Principal Biostatistician , Medical Affairs (FSP -Permanent Homebased)

IQVIA Commercial GmbH & Co. OHG

Key Responsibilities: Leadership: Serve as a biostatistical consultant for other members of the department and staff members from other Biostatistics departments within the company Represent sponsors at meetings with regulatory agencies or other regulatory meetings, may participate as a member of a Data and Safety Monitoring Committee Participate in independent research activities, teaching opportunities, presentations, and preparation of manuscripts for publication Participate as high level lead biostatistician on major projects, including developing/reviewing protocols, preparing analysis plans, and writing sections of joint clinical/statistical reports, integrated summaries and/or NDA sections Leading studies at an operational level Provide expert review and initiate methodology development work with regards to statistical standards and validation procedures Consult on operational/statistical/therapeutic area topics Knowledge Sharing: Maintain knowledge and awareness of developments in biostatistics and clinical trial methodology, and regulatory requirements that impact on analyses Performs as subject matter expert (SME) Risk Management: Identifies risks to project delivery and/or quality, leads in a way to minimize risks Anticipates risks to avert need for study level escalations, supports lead in implementing risk mitigation actions Lock and Unblinding Process: Leads the database lock and unblinding process for the statistical team Participate on the biostatistics randomization team (drafts randomization specifications and/or perform quality control (QC) review of randomization schedules) Statistical Expertise: Provide expert statistical input into review of statistical deliverables (i.e. statistical section of a protocol, statistical analysis plans, table shells, programming and table specifications, data review, tables, listings, figures, and statistical sections for complex and/or integrated reports) Provide expert input into data management deliverables (i.e. database design, CRF design, validation checks and critical data) Provide expert review of ADaM reviewers guide (ADRG) and metadata Perform senior biostatistical review (SBR) Produce or perform quality control review of sample size calculations for complex studies Requirements: Masters or PhD degree in Biostatistics or a related field with relevant experience within the life-science industry Expert in a broad range of complex statistical methods that apply to Phase 2-3 clinical trials Expert in strategically collaborating with clinical and drug development expertsExperience in serving as statistical lead for regulatory submissions, including preparation of submission datasets, eCTD support, meeting with regulatory teams, and responding to regulatory queries In-depth knowledge of applicable clinical research regulatory requirements, Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines Strong working knowledge of SAS or RExcellent knowledge of CDISC Data Standards Superb communication and collaboration skills Independent and pro-active problem solving skills IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries.

Reading, Berkshire, United Kingdom

(Junior) Sales & Alliance Manager Eastern Europe (m/f/d)

CHEPLAPHARM Arzneimittel GmbH

Berlin, Greifswald, Remote

Consultant

Deutsche Post AG

Cyberjaya, Selangor, Malaysia

Senior Consultant (m/w/d) – Value and Risk Advisory

Jones Lang LaSalle SE

Für unser Value and Risk Advisory Team in München, suchen wir Dich als Senior Consultant (m/w/d) – Value and Risk Advisory Das erwartet Dich Durchführung und Steuerung nationaler und internationaler Bewertungsprojekte für Immobilien und Portfolios Eigenverantwortliche Projektleitung von der Initiierung bis zum Abschluss Management von Ressourcen, Risiken und Prozessen Anwendung nationaler und internationaler Bewertungsverfahren (ImmoWertV / BelWertV, RICS, IVSC, TEGoVA) Erstellung von Wertgutachten und Marktanalysen in deutscher und englischer Sprache Enge Zusammenarbeit mit dem VRA-Produktteam zur Weiterentwicklung von Produkten und Daten Identifizierung von Cross-Selling-Möglichkeiten im Sinne von OneJLL Standortübergreifende Projektzusammenarbeit innerhalb von Deutschland und mit den Bewertungsteams in EMEA Was Du mitbringen solltest Abgeschlossenes Bachelor- oder Masterstudium (Immobilienwirtschaft, BWL, VWL, Bauingenieurwesen o.ä.) 2-3 Jahre Berufserfahrung in der Immobilienbewertung, insbesondere im Gewerbeimmobilienbereich Erste Schritte in Richtung HypZert F Qualifikation eingeleitet oder Interesse diese Qualifikation zeitnah zu erlangen Sehr gute MS-Office- und Englischkenntnisse Eigenverantwortliches Arbeiten und hohe Kundenorientierung Freude an der gemeinsamen Arbeit im Team und eine hohe Kundenorientierung Unser Angebot Auszeit und Erholung durch 30 Urlaubstage im Jahr und bis zu 10 Tage Bildungsurlaub Zugriff auf die globale JLL Weiterbildungsplattform zum gemeinsamen Entwickeln deines individuellen Karrierepfads Förderung von und Kostenübernahme für immobilienwirtschaftliche Fortbildungen und Mitgliedschaften (z.B.

Munich, DEU

Senior Quality Assurance Manager (m/w/d) - SCAYLE - onsite in Hamburg or Berlin

ABOUT YOU GmbH & Co. KG

Hamburg or Berlin (hybrid)

(Senior) Consultant Office Leasing (m/w/d)

Jones Lang LaSalle SE

Als (Senior) Consultant Office Leasing gestaltest Du die Zukunft der Arbeitswelten mit – von innovativen Start-up-Spaces bis zu prestigeträchtigen Corporate Headquarters.

Munich, DEU

(Senior) Sales and Alliance Manager Western Europe (m/f/d)

CHEPLAPHARM Arzneimittel GmbH

Berlin, Greifswald, Remote

(Senior) Sales & Alliance Manager Asia Pacific (m/f/d)

CHEPLAPHARM Arzneimittel GmbH

Berlin, Greifswald, Remote