Medical Affairs Effectiveness Specialist

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.

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...

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...

Job SummaryWe are seeking a highly skilled Regulatory Affairs Specialist to join our team at Hologic, Inc. The successful candidate will be responsible for ensuring compliance with regulatory requirements and guidelines for medical device registration.Key ResponsibilitiesEstablish and maintain registration plans for medical devices, ensuring compliance with...

About the Role:At UCB, we are committed to creating value for patients by pushing the boundaries of what is possible. We are seeking a Senior Medical Affairs Specialist with expertise in neurology to join our team.Key Responsibilities:Provide scientific support to internal stakeholdersKOL engagement and collaborationSupport clinical trial and development...

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...

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...

Key ResponsibilitiesAs a Medical Advisor - Insulin Specialist at Novo Nordisk, you will be responsible for developing and implementing regional medical strategies to ensure top-level medical contribution to internal and external customers. This includes managing key opinion leaders, leading regional medical projects, and ensuring medical and marketing...

Are you passionate about driving innovation in the pharmaceutical industry? Do you want to make a difference in the lives of patients? We are seeking a highly motivated and experienced Regulatory Affairs Specialist to join our team at Novo Nordisk.About the RoleDevelop and implement regulatory strategies to ensure compliance with global...

Are you passionate about driving innovation in the pharmaceutical industry? Do you want to make a meaningful impact on the lives of patients? Novo Nordisk A/S is seeking a talented Regulatory Affairs Specialist to join our team.The PositionDevelop and implement regulatory strategies for new products and submissionsCollaborate with cross-functional teams to...

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 the RoleWe are seeking a highly skilled Regulatory Affairs Manager to join our team at Galderma. As a key member of our regulatory team, you will be responsible for preparing and submitting regulatory applications to obtain approval for new products and existing license renewals and variations.Key ResponsibilitiesWork closely with cross-functional...

Key ResponsibilitiesAs a Regulatory Affairs Specialist at Novo Nordisk, you will be responsible for planning and executing regulatory strategies to ensure compliance with global regulations. This includes submissions and approvals for new products, license renewals, variations, and deregistrations.QualificationsRelevant graduate-level degree in a field such...

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...

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 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...

Job DescriptionWe are seeking a highly skilled Global Regulatory Affairs Leader to join our team at 1215 GlaxoSmithKline (China) Investment Co Ltd. As a key member of our organization, you will be responsible for providing strategic and technical regulatory support to our line manager.Key Responsibilities:Provide high-quality regulatory input and advice on...