Senior Manager, Regulatory Submissions Operations

Job Summary: We are seeking a highly experienced Senior Regulatory Submissions Project Manager to lead our Regulatory Submissions team. The ideal candidate will have a strong background in Regulatory Submissions, excellent leadership skills, and the ability to manage multiple projects simultaneously.Key Responsibilities:Lead a team of Regulatory Submissions...

Job SummaryWe are seeking a highly experienced Senior Regulatory Submissions Project Manager to lead our Regulatory Submissions delivery team within IQVIA Translations. The ideal candidate will have a strong background in Regulatory Submissions, excellent leadership skills, and the ability to drive process improvements.Key ResponsibilitiesLead a team of...

Regulatory Submissions Leadership OpportunityThe Associate Director – Regulatory Submissions is responsible for leading a worldwide Regulatory Submissions delivery team within IQVIA Translations. This team is in charge of developing and harmonizing the Regulatory Submissions Process.Key responsibilities include:Leading Regulatory submission Team Leaders...

Job SummaryThe Senior Manager Regulatory Submissions Process Development will lead a worldwide delivery team within IQVIA Translations. This team is responsible for developing and harmonizing the Regulatory Submissions Process. The ideal candidate will have experience working with QRDs, CTDs, SmPC, PIL, and other regulatory materials for EMA, SwissMedic,...

Regulatory Submissions Project ManagerThe ideal candidate will lead a worldwide Regulatory Submissions delivery team within IQVIA Translations. This team is responsible for the development and harmonization of the Regulatory Submissions Process. The successful candidate will have experience working with QRDs, CTDs, SmPC, PIL, and other regulatory materials...

Regulatory Submissions Director Job DescriptionThe Associate Director, Regulatory Submissions is responsible to lead a worldwide Regulatory Submissions delivery team within IQVIA Translations.Key Responsibilities:Lead a team of Regulatory Submission Team Leaders to ensure the whole team meets and exceeds their monthly and yearly goals and...

Regulatory Submissions CoordinatorWe are seeking a highly organized and detail-oriented Regulatory Submissions Coordinator to join our Clinical Operations team in Madrid. This role plays a critical part in the clinical trial management process at Medpace.Key Responsibilities:Prepare, review, and submit initial clinical trial applications to regulatory...

Regulatory Submissions CoordinatorWe are seeking a highly organized and detail-oriented Regulatory Submissions Coordinator to join our Clinical Operations team in Madrid. This role plays a critical part in the clinical trial management process at Medpace.Key Responsibilities:Prepare, review, and submit initial clinical trial applications to regulatory...

Regulatory Submissions Director Opportunity at IQVIAThis is a key role for a seasoned professional who can lead a team of project managers in regulatory submissions. The successful candidate will have experience in managing teams, processes, and projects in the life sciences industry.Responsibilities:Lead a team of project managers in regulatory...

Regulatory Submissions Project ManagerAt IQVIA, we are seeking a highly skilled Regulatory Submissions Project Manager to join our team. As a key member of our Project Management team, you will be responsible for coordinating and managing the full lifecycle of Regulatory Submissions translation and localization projects to completion.Key responsibilities...

Job Summary:Medpace, a leading clinical contract research organization, is seeking a full-time Regulatory Submissions Coordinator to join its Clinical Operations team in Madrid. This role plays a crucial part in the clinical trial management process, ensuring timely and compliant submissions to regulatory authorities and Ethics committees.Key...

Job Summary:Medpace, a leading clinical contract research organization, is seeking a full-time Regulatory Submissions Coordinator to join its Clinical Operations team in Madrid. This role plays a crucial part in the clinical trial management process, ensuring timely and compliant submissions to regulatory authorities and Ethics committees.Key...

Job SummaryWe are seeking a Regulatory Submissions Coordinator to join our Clinical Operations team in Madrid. This position plays a key role in the clinical trial management process at Medpace.ResponsibilitiesPrepare, review, and file initial clinical trial applications to regulatory authorities and Ethics committees;Ensure submissions comply with...

Job Title: Regulatory Submissions Project ManagerJob Summary:We are seeking a highly skilled Regulatory Submissions Project Manager to join our team at IQVIA. As a key member of our Project Management team, you will be responsible for coordinating and managing the full lifecycle of Regulatory Submissions translation and localization projects to...

Job Title: Regulatory Submissions Project ManagerAt IQVIA, we are seeking a highly skilled Regulatory Submissions Project Manager to join our team. As a key member of our Project Management team, you will be responsible for coordinating and managing the full lifecycle of Regulatory Submissions translation and localization projects to completion.Key...

Job SummaryMedpace is seeking a Regulatory Submissions Coordinator to join our Clinical Operations team in Madrid. This role plays a key part in the clinical trial management process, ensuring timely and compliant submissions to regulatory authorities and Ethics committees.ResponsibilitiesPrepare, review, and file initial clinical trial applications to...

Regulatory Submissions Project ManagerAt IQVIA, we are seeking a highly skilled Regulatory Submissions Project Manager to join our team. As a key member of our Project Management team, you will be responsible for coordinating and managing the full lifecycle of Regulatory Submissions translation and localization projects to completion.Key...

Job Summary:Medpace, a leading clinical contract research organization, is seeking a highly skilled Regulatory Submissions Coordinator to join its Clinical Operations team in Madrid. This role plays a critical part in the clinical trial management process, ensuring timely and compliant submissions to regulatory authorities and Ethics committees.This is an...

Job Summary:Medpace, a leading clinical contract research organization, is seeking a highly skilled Regulatory Submissions Coordinator to join its Clinical Operations team in Madrid. This role plays a critical part in the clinical trial management process, ensuring timely and compliant submissions to regulatory authorities and Ethics committees.This is an...

Clinical Operations at Medpace is growing rapidly, and we are seeking a full-time Regulatory Submissions Coordinator to join our team in Madrid. This role plays a key part in the clinical trial management process. If you want to develop your career further, this is the opportunity for you.Responsibilities:- Prepare, review, and file initial clinical trial...