Delivery & Operations Lead, IQVIA Regulatory Intelligence London, United Kingdom projects by:o Prioritize, scope and drive content improvement/enhancement projects to identify the relevant regulatory contento Contribute to the content identification and requirements and theRegulatory Affairs Project Manager / Regulatory Affairs Manager (m/f/d) Mannheim projects simultaneously Self-motivated and capable of working independently in a self-management environment Profound English and German skillsAffinity for IT and good MS Office skills 30 days leave perRegulatory Affairs Project Manager / Regulatory Affairs Manager (m/f/d) Mannheim projects simultaneously Self-motivated and capable of working independently in a self-management environment Profound English and German skillsAffinity for IT and good MS Office skills 30 days leave per, and provide clarifications to management Participate in projects and initiatives on demandManaging the tax reporting process with our local service providers and Group Tax, aligning deliverableHR Project & Change Management and Reporting Spezialist (m/f/d) Geneva . Moreover, you will receive detailed and prompt feedback from us.Mein ArbeitgeberFor one of our customer we are looking for an HR project and change manager You will prepare data and presentations related toHR Project & Change Management and Reporting Spezialist (m/f/d) Geneva . Moreover, you will receive detailed and prompt feedback from us.Mein ArbeitgeberFor one of our customer we are looking for an HR project and change manager You will prepare data and presentationsassurance and analysis, and provide clarifications to management Participate in projects and initiatives on demandManaging the tax reporting process with our local service providers and Group Tax, aligningRegulatory Manager, Clinical Trials Regulatory Management- Home-based, Europe Reading, Berkshire, United Kingdom Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently provides regulatory support for complex projects and programsRESPONSIBILITIESActs as aSenior Director, Regulatory Strategy Lead (home-based) Reading, Berkshire, United Kingdom for the development of regulatory business, in accordance with RADDS and Corporate business plans. Participates in project-related work, as necessary. Provide scientific, regulatory, and productManager Regulatory Affairs (m/f/d)* Mainz in regulatory affairs or medical devices, with a focus on interfaces with quality management.Proven skills in project management and ability to think interdisciplinary.Profound knowledge of the regulatoryRegulatory Affairs Manager - (Swiss Submissions, home-based) Frankfurt, Hesse, Germany register several of development projects into the international region. This role is key to driving both the Regulatory strategy and execution.• Provide Regulatory Consulting for ODS Applications, NewRegulatory and Start Up Manager (SAM)(FSP) Reading, Berkshire, United Kingdom , oversight of the scope of work, budget and resources.Essential FunctionsOversee the execution of Site Activation (including pre-award/bid defense activities) and/or Maintenance for assigned projectsRegulatory and Start Up Manager (SAM)(FSP) Belgrade, Serbia , oversight of the scope of work, budget and resources.Essential FunctionsOversee the execution of Site Activation (including pre-award/bid defense activities) and/or Maintenance for assigned projectsAssociate Manager, Clinical Trials Regulatory Management- Home-based, Europe Reading, Berkshire, United Kingdom Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently provides regulatory support for more complex projects.RESPONSIBILITIESActs as a Clinical TrialRegulatory Affairs Manager (f/m/d) Mannheim manage multiple projects simultaneously Self-motivated and capable of working independently in a self-management environmentRegulatory and Start Up Specialist 2 (FSP) (m/w/d) Home Based Frankfurt, Hesse, Germany (SOPs), project requirements and contractual/budgetary guidelines. May also include maintenance activities. At least 3 years' experience with submissions and CTIS experience. German and English fluentLocal Trial Manager or Senior LTM (m/w/d) Frankfurt, Hesse, Germany 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 providesCompliance & Governance Manager (m/f/d) Hamburg SCAYLE Payments You are responsible for (technical) compliance projectsRequirementsYou have minimum of 3-4 years' experience in the field of compliance in the Financial Service Industry or FinTechRegulatory Affairs Manager (f/m/d) Ludwigshafen market products internationally Coordinate and complete documents required by federal agencies, maintaining complex files and electronic document management systems and work with project teams to obtainSenior Statistical Programmer - Global BIOS Frankfurt, Hesse, Germany & Medical) team at IQVIA are experienced in submissions for all major regions; working together with key groups such as, Global Regulatory Affairs, Safety, Project and Data Management, and Medical Writing, tothe compliance with procedures globally Support the process of headcount budgeting, forecasting and strategic planning Contribute to strategic projects from an HR analytics and HR ControllingProject Manager - Protection and Resilience (m/f/d) Zurich pinpoint gaps in compliance with DORA requirements and devise strategies for gap mitigationImplement a Third Party Risk Management Framework based on the Allianz Group require-ments Project managementHead of New Product Development (abgeschlossen) Relevant project management experience, preferably in manufacturing Understanding of EU food regulatory environment Able to deal with and manage complexity, building strong relationships, striving for& Medical) team at IQVIA are experienced in submissions for all major regions; working together with key groups such as, Global Regulatory Affairs, Safety, Project and Data Management, and Medical Writing, toWerkstudent (m/w/d) Operations & Digital Project Management Mietwagen Augsburg Regulatory Affairs Manager (m/f) EMEA - Specialist who is able to make hands-on decisions and set-up a long term strategy (abgeschlossen) International projects, e.g. reducing complexity for product approvals, label management, ingredient acceptance and specification managementProviding practical solutions for the business, in a quick and efficientproper follow-up.Plans projects and measures to improve occupational safety, for example to implement BU-wide occupational safety programs or best practice and lessons learnt transfer to all BU•Interaction with PdS Countries teams globally (finances, proactive reporting, escalations, change management, central & local projects and initiatives, service alignment, eWB, … )•Providing analyses used by& Medical) team at IQVIA are experienced in submissions for all major regions; working together with key groups such as, Global Regulatory Affairs, Safety, Project and Data Management, and Medical Writing, toSafety Manager - San Antonio San Antonio,Texas Knowledge & experience to provide effective training on all appropriate safety related topics Ability to travel Excellent Computer skills Power point, Excel, Word, Visio and ProjectPreferred Requirementsenvironment; you have a strong understanding of liquid product properties and interations during industrial processing Strong project management skills and comfortable working in international project teams andGlobal Medical Trial Lead, Early Phase Clinical Trials (m/w/d) Frankfurt, Hesse, Germany The IQVIA Clinical Functional Service Partnerships (Clinical FSP) department is providing highly skilled professionals to our client's project team to set-up and execute clinical trials. Joining theproject deliverables with an emphasis on quality, productivity, and consistencyYour profile:1 to 3 years of experience required in SAC for various business departmentsAt least 1 full implementation ofProduct Regulatory and Compliance Engineer (f/m/dd) Manching Technik GmbH!Your TasksImplementation of the product regulatory & compliance process with regard to product safety Support of technical documentation within the development projects, in particularLaboratory Engineer for Analytical Testing Services Duryea usYou can expect interesting tasks and challenging projects, as well as motivated and friendly teams in fields that influence our future.Do you want to be successful with us? Pease submit yourfor respectful interaction, ethical behavior and integrity where sustainability mattersPotential to see your ideas realized and to make an impact on technically interesting projectsNew challenges andSenior Project Scheduler Johannesburg,Gauteng an advantage Primavera and MS Projects.Work Experience:Minimum of 10 years relevant experience in executing E / EP / EPCm / EPC contracts, preferably in the oil and gas, chemical and energy environmentsPrimavera and MS Projects.Work ExperienceMinimum of 5 - 10 years relevant experience in executing E / EP / EPCm / EPC contracts, preferably in the oil and gas, chemical and energy environments Experience#J-18808-Ljbffr
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