Senior Global Program Regulatory Manager

Senior Global Program Regulatory ManagerJob ID REQ-10043957Mar 19, 2025Summary-Directs the development of submission of product registration, progress reports, supplements, amendments, and/or periodic experience reports. Provides strategic product direction to teams on interaction and negotiates evidence with regulatory agencies. Interacts and negotiates...

Job OverviewThe role of the Senior Global Program Regulatory Manager is to oversee the development and implementation of regulatory strategies for product registration, progress reports, supplements, amendments, and periodic experience reports. This position requires a strong understanding of global regulatory requirements and the ability to provide...

We are a company driven by innovation to create a healthier future. With over 100,000 employees worldwide working together to achieve scientific progress and ensure that everyone has access to healthcare – today and for future generations.About the RoleThe Regulatory Program Director is responsible for developing and driving regulatory strategies for...

Job Description SummaryDirects the development of submission of product registration, progress reports, supplements, amendments, and/or periodic experience reports. Provides strategic product direction to teams on interaction and negotiates evidence with regulatory agencies. Interacts and negotiates with regulatory agency personnel in order to expedite...

About the RoleWe are seeking an experienced Senior Global Program Regulatory Manager to join our team at Novartis Farmacéutica. In this role, you will be responsible for implementing regulatory strategy and managing operational activities for assigned major/large regions. You will also provide input into global regulatory strategy and contribute to...

< < ZURÜCKBEWERBENvon: Innovative Medicines Summary-Directs the development of submission of product registration, progress reports, supplements, amendments, and/or periodic experience reports. Provides strategic product direction to teams on interaction and negotiates evidence with regulatory agencies. Interacts and negotiates with regulatory agency...

Job Description SummaryDirects the development of submission of product registration, progress reports, supplements, amendments, and/or periodic experience reports. Provides strategic product direction to teams on interaction and negotiates evidence with regulatory agencies. Interacts and negotiates with regulatory agency personnel in order to expedite...

-Directs the development of submission of product registration, progress reports, supplements, amendments, and/or periodic experience reports. Provides strategic product direction to teams on interaction and negotiates evidence with regulatory agencies. Interacts and negotiates with regulatory agency personnel in order to expedite approval of pending...

The Senior Program Manager - Pharmaceutical Safety at Novartis Farmacéutica oversees overall signal detection, monitoring, evaluation, interpretation, and appropriate management of safety information. This role is part of our Radioligand Therapy team and requires a strong expertise in drug development, clinical trial methodology, regulatory requirements,...

We are seeking a highly skilled Senior Clinical Development Manager to join our team. In this role, you will be responsible for driving the development and execution of clinical development strategies, collaborating with internal and external stakeholders to optimize trial designs and study protocols, and providing medical expertise and oversight throughout...

The Life Science Career NetworkCTC specializes in helping companies find top talent and offers reliable HR, consulting services, and skill development programs. We support candidates in advancing their careers and provide the latest training to stay competitive.Our client, a global pharmaceutical leader headquartered in Basel, Switzerland, is undergoing a...

Regulatory Affairs Global Labelling Manager12 hours ago Be among the first 25 applicantsDirect message the job poster from Coopers Group AGTalent Acquisition Consultant at Coopers Group AG - Life ScienceEnd date: 31.08.2025Can be fully remoteThe RA Global Labelling Manager is responsible for the creation and maintenance of regulatory compliant, competitive,...

Senior Program Manager OpportunityWe are seeking a highly skilled Senior Program Manager to join our team.The successful candidate will have extensive experience in leading large-scale digitalization projects and deep knowledge of digital transformation technologies and frameworks.This role offers a unique opportunity to work on a complex project in the...

Key ResponsibilitiesThe Global Regulatory Compliance Manager is responsible for ensuring that all regulatory processes are compliant with global regulations and Novartis standards.This includes monitoring and reviewing emerging regulations and regulatory guidelines, analyzing their impact on Novartis regulatory processes, and contributing to inspections and...

About the RoleThe Director Equity Rewards & Employment Tax will play a critical role in driving Sandoz's global equity program forward. This includes overseeing the design, implementation, and administration of equity plans, as well as ensuring compliance with regulatory requirements.Your Key Accountabilities:Develop and maintain relationships with key...

5 days ago Be among the first 25 applicantsGet AI-powered advice on this job and more exclusive features.The Life Science Career Network: CTC specializes in helping companies find top talent, providing HR, consulting services, and skill development programs. We help candidates advance their careers with the latest training to stay competitive.About Our...

Job DescriptionThe Director of Employee Incentives is responsible for overseeing all aspects of equity plan management, including governance, compliance, vendor management, and process improvements. This role requires a strong background in equity rewards and employment tax, with experience working in multinational companies.The ideal candidate will be able...

At Roche, we are committed to advancing science and ensuring everyone has access to healthcare today and for generations to come.About the RoleWe are seeking a skilled Regulatory Program Director to join our team. As a key member of our regulatory affairs department, you will be responsible for developing and driving regulatory strategies for combination...

We're looking for a driven Global Regulatory Strategy Manager to lead our efforts in developing and implementing effective regulatory strategies for devices and ensure compliance with domestic and international regulations.Main ResponsibilitiesDevelop and drive regulatory strategies for combination products and standalone physical devices.Work closely with...

Global Program Clinical Head - CRMGlobal Program Clinical Head - CRMApply locations Basel (City) time type Full time posted on Posted 30+ Days Ago job requisition id REQ-10003153BandLevel 7Job Description SummaryThe Global Program Clinical Head (GPCH) is the global clinical leader responsible for one or more clinical programs across indications, involving...