Translation Project Manager – Regulatory Submissions
hace 4 días
TRANSLATION PROJECT MANAGER REGULATORY SUBMISSIONSWorking with the wider Project Management team, the Translation Project Manager Regulatory Submissions is responsible for coordinating and managing the full lifecycle of Regulatory Submissions translation and localization projects to completion whilst ensuring IQVIA's standards are met.Manage multiple Regulatory Submissions translation and localization projects at any one time from receipt to completionLiaise with the client to assess and agree project parameters and requirementsAssess project scope to select appropriate vendors and negotiate deadlines effectivelyEstablish and maintain excellent relationships with freelance and in house linguists globallyMonitor and manage the status of assigned projects to effectively anticipate and prevent issuesAccurately complete project finances including quoting and budgetingPrepare and maintain project documentation and informationUnderstand and adhere to the Quality Management SystemComply with relevant and applicable IQVIA procedures and SOPsAssist in the maintenance of linguistic assets including glossaries and style guidesEnsure that high quality is maintained for all projects through QA checksProvide weekend coverage in case needed due to project scheduleRequirements :Minimum of 2 years of experience working in Project Management in the Language Services industryMinimum of 1 year of experience working in Regulatory Submissions Project Management in the Language Services industryBachelor's degree, ideally in a linguistic, business or scientific fieldFluency in English is essential, an additional language would be advantageousExcellent written / verbal communication skillsExcellent attention to detail to ensure that high quality standards are maintainedAbility to meet strict deadlines and to manage competing priorities and changing demandsExcellent problem solving and analytical skillsAbility to follow instructions and work independently whilst using own initiativeDemonstration of advanced IT skillsExperience working with TMS and CAT tools, experience working with XTRF and / or memoQ would be highly advantageousAbility to establish and maintain effective working relationships with colleagues, managers and clientsIQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry.We believe in pushing the boundaries of human science and data science to make the biggest impact possible to help our customers create a healthier world. Learn more at#J-18808-Ljbffr
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Madrid, Madrid, España IQVIA A tiempo completoTRANSLATION QC JUNIOR PROJECT MANAGER – REGULATORY SUBMISSIONSWorking with the Regulatory Submissions Project Management team, the Translation QC Project Manager – Regulatory Submissions is responsible for coordinating and performing the QC step for the Regulatory Submissions translation and localization projects whilst ensuring IQVIA's standards are...
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Madrid, Madrid, España IQVIA A tiempo completoTRANSLATION QC JUNIOR PROJECT MANAGER – REGULATORY SUBMISSIONSWorking with the Regulatory Submissions Project Management team, the Translation QC Project Manager – Regulatory Submissions is responsible for coordinating and performing the QC step for the Regulatory Submissions translation and localization projects whilst ensuring IQVIA's standards are...
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Madrid, Madrid, España Iqvia A tiempo completoThe Associate Director – Regulatory SubmissionsThe Associate Director – Regulatory Submissions is responsible to lead a worldwide Regulatory Submissions delivery team within IQVIA Translations. This team is in charge of the development and harmonization of the Regulatory Submissions Process. The Associate Director – Regulatory Submissions has...
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Madrid, España Sdi Digital Group A tiempo completoThe Associate Director Regulatory Submissions is responsible to lead a worldwide Regulatory Submissions delivery team within IQVIA Translations. This team is in charge of the development and harmonization of the Regulatory Submissions Process. The Associate Director Regulatory Submissions has experience working with QRDs, CTDs, SmPC, PIL and any other...
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Madrid, Madrid, España Iqvia A tiempo completoThe Associate Director – Regulatory SubmissionsThe Associate Director – Regulatory Submissions is responsible to lead a worldwide Regulatory Submissions delivery team within IQVIA Translations. This team is in charge of the development and harmonization of the Regulatory Submissions Process. The Associate Director – Regulatory Submissions has...
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Madrid, Madrid, España Iqvia A tiempo completoThe Associate Director – Regulatory SubmissionsThe Associate Director – Regulatory Submissions is responsible to lead a worldwide Regulatory Submissions delivery team within IQVIA Translations. This team is in charge of the development and harmonization of the Regulatory Submissions Process. The Associate Director – Regulatory Submissions has...
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Madrid, Madrid, España Iqvia A tiempo completoThe Associate Director – Regulatory SubmissionsThe Associate Director – Regulatory Submissions is responsible to lead a worldwide Regulatory Submissions delivery team within IQVIA Translations. This team is in charge of the development and harmonization of the Regulatory Submissions Process. The Associate Director – Regulatory Submissions has...
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Madrid, España IQVIA A tiempo completoThe Associate Director – Regulatory Submissions is responsible to lead a worldwide Regulatory Submissions delivery team within IQVIA Translations. This team is in charge of the development and harmonization of the Regulatory Submissions Process. The Associate Director – Regulatory Submissions has experience working with QRDs, CTDs, SmPC, PIL and any...
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Madrid, Madrid, España SDi Digital Group A tiempo completoThe Associate Director Regulatory Submissions is responsible to lead a worldwide Regulatory Submissions delivery team within IQVIA Translations.This team is in charge of the development and harmonization of the Regulatory Submissions Process. The Associate Director Regulatory Submissions has experience working with QRDs, CTDs, SmPC, PIL and any other...
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Madrid, España IQVIA A tiempo completoThe Associate Director – Regulatory Submissions is responsible to lead a worldwide Regulatory Submissions delivery team within IQVIA Translations. This team is in charge of the development and harmonization of the Regulatory Submissions Process. The Associate Director – Regulatory Submissions has experience working with QRDs, CTDs, SmPC, PIL and any...
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Madrid, Madrid, España IQVIA LLC A tiempo completoAssociate Director, Regulatory Submissions Project Management page is loaded Associate Director, Regulatory Submissions Project Management Apply locations Reading, Berkshire, United Kingdom Madrid, Spain time type Full time posted on Posted Yesterday job requisition id R The Associate Director – Regulatory Submissions is responsible to lead a worldwide...
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Madrid Centro, Madrid, España Iqvia A tiempo completoThe Associate Director – Regulatory SubmissionsThe Associate Director – Regulatory Submissions is responsible to lead a worldwide Regulatory Submissions delivery team within IQVIA Translations. This team is in charge of the development and harmonization of the Regulatory Submissions Process. The Associate Director – Regulatory Submissions has...
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Madrid, Madrid, España Iqvia A tiempo completoThe Associate Director – Regulatory SubmissionsThe Associate Director – Regulatory Submissions is responsible to lead a worldwide Regulatory Submissions delivery team within IQVIA Translations. This team is in charge of the development and harmonization of the Regulatory Submissions Process. The Associate Director – Regulatory Submissions has...
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Madrid, España Iqvia A tiempo completo.The Associate Director – Regulatory SubmissionsThe Associate Director – Regulatory Submissions is responsible to lead a worldwide Regulatory Submissions delivery team within IQVIA Translations. This team is in charge of the development and harmonization of the Regulatory Submissions Process. The Associate Director – Regulatory Submissions has...
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(Translation) Associate Project Manager
hace 4 días
Madrid, España Iqvia Llc A tiempo completo.(Translation) Associate Project Manager page is loaded (Translation) Associate Project Manager Apply locations Madrid, Spain Porto Salvo, Portugal Barcelona, Spain time type Full time posted on Posted 2 Days Ago job requisition id R1421842 IQVIA is looking for a motivated and detail-oriented Associate Project Manager to manage the translation development...
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(Translation) Associate Project Manager
hace 4 días
Madrid, España Iqvia A tiempo completo.IQVIA is looking for a motivated and detail-oriented Associate Project Manager to manage the translation development projects of Clinical Outcomes Assessments (COAs).Job SummaryThe Associate Project Manager will be responsible for managing the lifecycle of COA cultural adaptation. The ideal candidate will support the management of translation and linguistic...
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(Translation) Associate Project Manager
hace 4 días
Madrid, España Iqvia Argentina A tiempo completo.IQVIA is looking for a motivated and detail-oriented Associate Project Manager to manage the translation development projects of Clinical Outcomes Assessments (COAs).Job SummaryThe Associate Project Manager will be responsible for managing the lifecycle of COA cultural adaptation. The ideal candidate will support the management of translation and linguistic...
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Translation Project Manager
hace 1 semana
Madrid, Madrid, España SMG Languages A tiempo completoStudio Moretto Group Srl, a multinational translation company, is looking for n. 1 Junior Translator Project Manager to hire for the London office in Fleet Street.What we are looking for: Junior Project Manager for a parttime role with real possibility to increase working hours as the business grows; Degree in Translation or Modern languages; Ideally...
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Madrid, España Iqvia A tiempo completo.Prepares and / or reviews regulatory documents to support clinical trial submissions. Independently provides regulatory support for complex projects and programsRESPONSIBILITIESActs as a Clinical Trial Regulatory Manager (CTRM) on complex clinical trial projects or programs and may act as a Regulatory Oversight for a key customerAbility to administratively...
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Regulatory Manager
hace 4 días
Madrid, España Oak HcFt A tiempo completo.Precision for Medicine (CRO) are recruiting a Regulatory Manager to join our team, candidates can be based in the following countries: UK, Spain, Hungary, Slovakia, Serbia, Romania or Poland.Position Summary:The Regulatory Manager (RM) provides regulatory strategy and development guidance for optimal conduct of clinical trials, regulatory agency meetings,...
