erste Erfahrung in der Führung und Entwicklung von Projektteams, auch ohne disziplinarische Weisungsbefugnis, sowie Kenntnisse in Teamentwicklung und Feedbackkultur. Sicherer Umgang mit Projektmanagement-Tools wie Microsoft Project, Azure DevOps, Visualisierungstools (z.B. Miro) und fundierte Methodenkenntnisse zur Ergänzung der COSMO CONSULT Projektmethodik.
Joining the Data Science & Advanced Analytics team provides the opportunity to work with large and complex data and methodologies in a fast-paced, ever-changing environment to support international customers. As a member of our team you can expect exciting international projects with interesting development perspectives. Why Join? Those who join us become part of a recognized global leader still willing to challenge the status quo to improve patient care.
Job Overview: As an Associate Director, Biostatistics, with regional/site presence, you will manage a team of Biostatistics staff and fulfil the role of site head or functional head within a site. You will provide direction and guidance in carrying out project assignments, interfacing with clients and other internal departments, and applying advanced statistical methods to project work.
Außerdem verantworten Sie das Monitoring und Reporting des Deployment-Fortschritts am Standort und nehmen regelmäßig an den Project Support Community Meetings teil. Ihr Profil: Must-haves Abgeschlossenes Studium im Bereich Life Sciences, Pharmazie, Biologie, Chemie oder Regulatory Affairs – oder vergleichbare Qualifikation mit Berufserfahrung; auch als Regulatory Affairs Specialist (m/w/d), Regulatory Operations Specialist (m/w/d) oder RIM Data Specialist (m/w/d) sind Sie willkommen.
Außerdem verantworten Sie das Monitoring und Reporting des Deployment-Fortschritts am Standort und nehmen regelmäßig an den Project Support Community Meetings teil. Ihr Profil: Must-haves Abgeschlossenes Studium im Bereich Life Sciences, Pharmazie, Biologie, Chemie oder Regulatory Affairs – oder vergleichbare Qualifikation mit Berufserfahrung; auch als Regulatory Affairs Specialist (m/w/d), Regulatory Operations Specialist (m/w/d) oder RIM Data Specialist (m/w/d) sind Sie willkommen.
You will provide internal consulting services, including specifications and user needs analysis for complex project or client requirements. Key Responsibilities: • Perform, plan co-ordinate, and implement the following for complex studies: - The programming, testing, and documentation of statistical programs for use in creating statistical tables, figures, and listing - The programming of analysis datasets (derived datasets) and transfer files for internal and external clients - The programming quality control checks for the source data and to report the data issues periodically • Ability to interpret project level requirements and develop programming specifications, as appropriate, for complex studies. • Provide advanced technical expertise in conjunction with internal and external clients, and independently bring project solutions to SP teams • Fulfil project responsibilities at the level of technical team lead for single complex studies or group of studies. • Directly communicate with internal and client statisticians and clinical team members to ensure appropriate understanding of requirements and project timelines • Estimate programming scope of work, manage resource assignments, communicate project status and negotiate/re-negotiate project timelines for deliverables • Use and promote the use of established standards, SOP and best practices • Provide training and mentoring to SP team members Requirements: • Bachelor's Degree in Maths, Computer science, Statistics, or related field • 7+ years’ Statistical Programming experience within the Life Science Industry • Strong Efficacy experience • Advanced knowledge of statistics, programming and/or clinical drug development process • Advanced knowledge of computing applications such as Base SAS, SAS Graph and SAS Macro • Language • Advanced knowledge of relevant Data Standards (such as CDISC/ADaM/SDTM) Join IQVIA to see where your skills can take you • Global exposure • Variety of therapeutic areas • Collaborative and supportive team environment • Access to cutting-edge and innovative, in-house technology • Excellent career development and progression opportunities • Work-Life Balance, with a strong focus on a positive well-being Unleash your potential!
The IQVIA sponsor-dedicated Clinical Functional Service Partnerships (Clinical FSP) department is supporting our client’s project team in the execution of clinical trials. Joining the team provides the opportunity to work with the preparation and documentation of clinical research projects in different therapeutic areas.
The IQVIA sponsor-dedicated Clinical Functional Service Partnerships (Clinical FSP) department is supporting our client’s project team in the execution of clinical trials. Joining the team provides the opportunity to work with the preparation and documentation of clinical research projects in different therapeutic areas in Germany or the DACH region.
You’ll have the opportunity to put your passions to work in an environment designed to help you gain experience in a wide variety of therapeutic areas and in covering projects in Germany, Austria and Switzerland. Your responsibilities will include: Performing site selection, initiation, monitoring and close-out visits.
IHRE AUFGABEN UND VERANTWORTUNGSBEREICHE: Projektmanagement eines anspruchsvollen und bekannten Großprojekts Projektleitungsfunktion gegenüber und Regelabstimmung mit dem Kunden Wöchentliche interne Projektbesprechungen mit dem Team sowie Durchführung der ARGE-Sitzungen Mitarbeiterführung, Ressourcenplanung und Recruiting, fachlicher und menschlicher Ansprechpartner und Support für das Projektteam Erstellung von Monatsberichten und Durchsprache mit den Beteiligten Steuerung von Terminen, Kosten und Qualitäten, Identifizierung und Lösung von Risiken für den Ablauf Mitverantwortung bei der technischen, wirtschaftlichen und organisatorischen Bauberatung Kommunikation, Information und Abstimmung mit allen Projektbeteiligten im gesamten Projektverlauf, Entscheidungen über die strategische Vorgehensweise IHRE QUALIFIKATION: Abgeschlossenes Studium der Architektur, Bauingenieurwesen oder eine vergleichbare Qualifikation Mehrjährige Berufserfahrung im Projektmanagement von großen Bauprojekten Mehrjährige Führungserfahrung in Projektteams Sehr gute Kenntnisse in HOAI, AHO, VOB und VgV sowie gute Kenntnisse im Umgang mit MS Project Gute Englischkenntnisse in Wort und Schrift Kompetenz in der Entwicklung innovativer Lösungen für technische und ökonomische Aufgabenstellungen sowie ein überzeugendes Auftreten UNSER KUNDE BIETET: Eigene Akademie mit vielfältigen Angeboten Mobiles Arbeiten (positionsabhängig), unterschiedliche Teilzeitmodelle, Kinderbetreuungszuschuss Firmenrad-Leasing und ÖPNV-Zuschuss Gesundheitsbonus für sportlich Aktive, moderne und ergonomische Arbeitsplätze Zugang zum Corporate-Benefits-Portal, kostenlose Getränke und frisches Obst Mitarbeiterempfehlungs-Programm, Networking-Events, Teamworkshops IHRE BERATER: Thorsten Augusti Tel: +49 228 25 90 4 - 0 Mail: t.augusti@fmsgmbh.de Andreas Hodapp-Schneider Tel: +49 228 25 90 4 - 17 Mail: a.hodapp@fmsgmbh.de Bitte geben Sie bei Ihrer Bewerbung per Mail die Kennziffer 20235 an!
The IQVIA™ Internship provides you with the opportunity to gain relevant, project-based work experience at one of the most successful and cutting-edge global clinical research units in the market while building relationships within the company that will impact your future.
The IQVIA™ Internship provides you with the opportunity to gain relevant, project-based work experience at one of the most successful and cutting-edge global clinical research units in the market while building relationships within the company that will impact your future.
Ob für private Investoren oder für die öffentliche Hand gebaut werden soll oder ob es um die Realisierung von Infrastrukturprojekten oder Hotels, um Quartiersentwicklung oder einen neuen Produktionsstandort für die Life Science-Industrie geht, unser Kunde möchte einen echten Mehrwert für Investoren, Bauherren und Nutzer schaffen IHRE AUFGABEN UND VERANTWORTUNGSBEREICHE: Projektmanagement von anspruchsvollen Projekten, von der Entwurfsplanung über die Ausschreibung, Vergabe bis hin zur Bauüberwachung und Inbetriebnahme Übernahme der Teilprojektleitung und stellvertretenden Projektleitung Erstellung von Machbarkeitsstudien und Wirtschaftlichkeitsbetrachtungen Steuerung von Terminen, Kosten und Gebäudequalitäten Mitverantwortung bei der technischen, wirtschaftlichen und organisatorischen Bauberatung Kommunikation, Information und Abstimmung mit allen Projektbeteiligten im gesamten Projektverlauf IHRE QUALIFIKATION: Abgeschlossenes Studium der Fachrichtung Bauingenieurwesen, Wirtschaftsingenieurwesen, Architektur oder eine vergleichbare Qualifikation Mindestens 2 Jahre Berufserfahrung im Projektmanagement von Bauprojekten Sehr gute Kenntnisse in HOAI, AHO, VOB und VgV sowie gute Kenntnisse im Umgang mit MS Project Gute Englischkenntnisse in Wort und Schrift Bereitschaft zu projektabhängigen Reisen im Inland und Ausland UNSER KUNDE BIETET: Eigene Akademie mit vielfältigen Angeboten Mobiles Arbeiten (positionsabhängig), unterschiedliche Teilzeitmodelle, Kinderbetreuungszuschuss Firmenrad-Leasing und ÖPNV-Zuschuss Gesundheitsbonus für sportlich Aktive, moderne und ergonomische Arbeitsplätze Zugang zum Corporate-Benefits-Portal, kostenlose Getränke und frisches Obst Mitarbeiterempfehlungs-Programm, Networking-Events, Teamworkshops IHR BERATER: Annemarie Steinhauer-Ahrens Tel: +49 228 25 90 4 - 20 Mail: a.steinhauer@fmsgmbh.de Bitte geben Sie bei Ihrer Bewerbung per Mail die Kennziffer 20223 an!
Stellenbeschreibung DEKRA Arbeit GmbH is seeking a dedicated and reliable Project Assistant (m/f/d) – Finance (AMLA) for a financial authority in Frankfurt am Main. In this role, you will support both the Governance team and IT Project Managers with administrative tasks, coordination of meetings and stakeholders, as well as project-related activities, ensuring timely execution and compliance with internal procedures.
Essential Functions Develop Coordinate the development of investigator grants and estimates, contracting strategies and proposal text to support the proposal development process.Develop contract language, payment language and budget templates as required as applicable to the positionUtilize and maintain contracting systems, tools, processes, and training materials for selected sponsors, studies or multi-protocol programs according to the Scope of Work and Project Plan, within the agreed project strategy.Ensure collaboration, including communication with sponsors, stakeholders and RSU regions and countries as applicable to the position, to successfully deliver the agreed project scope in compliance with sponsor requirements and/or the RSU Management Plan.Provide specialist legal, operational and financial contracting support to the Study Teams, as applicable to site agreements to facilitate efficient business development and initiation and maintenance of clinical trials, whilst enabling compliance with regulatory requirements.Ensure overall contracting efficiency and adherence to project timelines and financial goals as applicable to site agreementsReport contracting performance metrics and out of scope contracting activities as required.Work with Quality Management to ensure appropriate contract management and quality standards.
The IQVIA sponsor-dedicated Clinical Functional Service Partnerships (Clinical FSP) department is supporting our client’s project team in the execution of clinical trials. Joining the team provides the opportunity to manage Early Phase clinical research projects in different therapeutic areas and to cooperate closely with one of our key clients.
Study Physician services Medical Content Oversight: Responsible for medical content in Clinical Trial Protocols (CTPs).Collaborates with Project Management, Patient Safety, Medical Writers, and trial/evidence teams.Provides medical input for CTP updates. Risk-Based Quality Management: Defines medically critical data/processes and associated risks.Contributes to Integrated Quality and Risk Management Plan (IQRMP).Participates in risk discussions during trial conduct.
YOUR ROLE Responsible for growing the long-term value and performance of the entire bread category by developing a category strategy to analyze and optimize the profitability of the product line Managing and coaching 2 Product Leaders Supporting OpCo’s in making strategic product choices, acting as an internal advisor and decision driver for the category Maintaining the standard portfolio, developing and maintaining strategic brands and concepts across multiple countries Leading innovations projects from business case to market introduction by customers, end-to-end (E2E) Building solid bridges between the group, organization and OpCo’s and co-create with cross functional colleagues Identifying additional markets to launch and defining with OpCo’s, M&A and strategic partnership options to address adjacent growth opportunities and complete the category portfolio Collaborating intensively with the other Global Category Managers, Product Leaders, the Commercial Development Manager and the OpCo’s Member of the Marketing/R&D Management Team and reporting to the Group Marketing/R&D Director YOUR PROFILE BSc/MSc degree in Marketing, Business Administration, Food Science & Technology or similar Relevant experience in international B2B marketing, category management in senior management roles, preferably in the international food ingredients industry Capable of understanding the technical aspects of products like functional ingredients such as enzymes, emulsifiers or other raw materials Strong project management skills by leading and participating in cross-functional teams and by building bridges between global and local teams Good understanding about trends, market and customer requirements and able to translate these into plans and actions Comfortable working in an international matrix organisation with different stakeholders, markets and cultures and willingness to travel in Europe; Zeelandia offers the possibility for hybrid working in combination with working in the office in Zierikzee or any other Zeelandia office or plant in Europe Excellent communication and presentation skills in English Personal skills: leadership, well organised, analytically strong, drive for innovation, setting priorities, convincing and taking decisions priorities, convincing and taking decisions CONTACT If you are interested in this position, please contact Jakob Jan Verbraak from our IFR-A partner DUPP, telephone: +31 317-468686 / +31 6-51820349 or apply through their website www.dupp.nl or e-mail your written application to info@dupp.nl.
The IQVIA sponsor-dedicated Clinical Functional Service Partnerships (Clinical FSP) department is supporting our client’s project team in the execution of clinical trials. Joining the team provides the opportunity to work with one single client and to manage clinical research projects in different therapeutic areas.
Support preparation of customer and bid defense meetings, e.g. training and preparation of the assigned project team; provide specific content; ensure presentation focus and content effectively conveys CAGT strategy. Attends and presents at customer meeting, or bid defense or partnership meetings, as required.