Senior Medical Affairs Specialist Neurology

Creating Value for PatientsWe are seeking a Medical Science Liaison to support our Medical Affairs team in the field of rare diseases.Key ResponsibilitiesKOL EngagementProvide internal scientific supportSupport clinical trial and development programsRequirementsMaster of clinical medicine, bio-pharmaceutical or related fieldMore than 1 year clinical...

Job OverviewPfizer is seeking a Medical Affairs Effectiveness Specialist - China Compliance Expert to join our team. This role will be responsible for reviewing China EG / Corp. Sponsorship/oversea meeting, in order to control and manage external funding risk through effective models and procedure.

Job SummaryWe are seeking a highly skilled Regulatory Affairs Specialist to join our team at Hologic, Inc. This role will be responsible for establishing and maintaining registration plans for medical devices, forecasting and managing project budgets, and coordinating submissions to regulatory agencies.Key ResponsibilitiesDevelop and execute registration...

Hologic, Inc. is seeking a highly skilled Regulatory Affairs Specialist to join our team.Job DescriptionThe ideal candidate will have more than 5 years of experience in regulatory affairs and related QA working experience in the medical device field.We are looking for someone who is familiar with imaging, surgical or IVD products and has a strong attention...

Job SummaryWe are seeking a highly skilled Life Sciences Medical Affairs Manager to join our team at IQVIA. The successful candidate will have a strong background in medical sciences and experience in developing relationships with healthcare professionals.Key ResponsibilitiesDevelop and maintain peer-to-peer scientific relationships with external thought...

Requirements and ResponsibilitiesThe Medical Affairs Effectiveness Lead will be responsible for reviewing China EG/CORP sponsorship and overseas meeting to control and manage external funding risk through effective models and procedures. He/she will work closely with the internal control, legal, and corporate compliance team to improve the pre-approval...

About the RoleWe are seeking a highly skilled Regulatory Affairs Professional to join our team at AbbVie. As a key member of our medical device regulatory affairs group, you will play a critical role in ensuring compliance with regulations and securing product approvals.

Role Overview:We are seeking a highly motivated and experienced Regulatory Affairs Specialist to join our team at GSK China. As a key member of our regulatory affairs team, you will be responsible for providing strategic and technical regulatory support to our line manager to ensure timely and high-quality submission and approval of our products in the...

Elevate Your Career with UCBWe are seeking a skilled Medical Science Liaison to join our team and contribute to our mission of creating value for patients.About the RoleDevelop and maintain relationships with key opinion leadersProvide internal scientific support and expertiseSupport clinical trial and development programsRequirementsMaster's degree in...

Job Overview:We are seeking an accomplished Senior Medical Director to lead our regional growth strategy and drive top-level medical contributions to internal and external customers.About the Role:Develop a comprehensive regional medical strategy that ensures alignment with business objectives.Collaborate with key opinion leaders (KOLs) to foster strong...

Job SummaryThis role requires a highly skilled and experienced professional to oversee the medical device regulatory compliance process in China. The successful candidate will be responsible for ensuring that all products meet the required regulatory standards and will work closely with the global team to achieve this goal.Key ResponsibilitiesDevelop and...

About Novo NordiskWe are a leading global healthcare company that is driven by one purpose – to make a difference for people living with diabetes, obesity and other serious chronic conditions.Job SummaryWe are seeking an experienced professional to join our Market Access and Public Affairs Department as Senior Director of Public Affairs and Sustainability....

About the RoleWe are seeking a highly motivated and experienced Regulatory Affairs professional to join our team at Novo Nordisk A/S. As a key member of our Clinical Medical Regulatory and Quality department, you will play a critical role in driving innovation and transforming the treatment paradigm for chronic diseases.Key ResponsibilitiesDevelop and...

About the RoleAs a Senior Technical Support Specialist, you will play a crucial role in ensuring the success of our medical devices in the Beijing region. You will be responsible for providing exceptional support to clients, training hospital technicians, and driving the adoption of our products.Key ResponsibilitiesDeliver top-notch technical support to...

Key ResponsibilitiesDevelop and implement regional medical strategies to ensure top-level medical contributions to internal and external customers.Manage key opinion leaders (KOLs) in the region to drive medical innovation.Lead regional medical projects, including IIS initiatives, to advance medical knowledge and practices.RequirementsMedical degree or...

Key Responsibilities:Develop a regional medical strategy that aligns with Novo Nordisk’s goals and objectives, ensuring top-level medical contribution to internal and external customers.Manage relationships with key opinion leaders (KOLs) in the region.Lead regional medical projects, including the development of medical content and materials.Knowledge,...

Job DescriptionWe are seeking a highly skilled Senior Regulatory Affairs Professional to join our team at Novo Nordisk.About the RoleThe successful candidate will be responsible for providing strategic regulatory guidance and support to ensure compliance with all relevant regulations and guidelines. This will include planning and executing regulatory...

Job SummaryAs a Medical Science Liaison (MSL) Manager for Takeda, you will be responsible for overseeing the strategic planning and execution of medical activities across various regions. This role requires a strong understanding of medical affairs, people management, and leadership skills to navigate complex projects and teams.Key Responsibilities1. Medical...

Key Responsibilities:As a Senior Regulatory Affairs CMC Manager at 1215 GlaxoSmithKline (China) Investment Co Ltd, you will be responsible for providing strategic and technical regulatory input for the purpose of commencing and maximizing GSK China business by facilitating the CMC submission and approval in a timely and high-quality manner.Key...

About the RoleWe are seeking a Senior Manager CMC Regulatory Affairs Professional to join our team at 1215 GlaxoSmithKline (China) Investment Co Ltd.Job SummaryThis role is responsible for providing strategic and technical regulatory input for new and established products, ensuring timely and high-quality CMC submissions and approvals in China.Key...