Medical Affairs Effectiveness

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 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 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.

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...

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 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...

Are you motivated by driving innovation for the life-changing benefit of patients? Are you ready to help transform the treatment paradigm for a broad range of chronic diseases that currently rely on injection-based therapies? Then this is your moment. Apply now and join Novo Nordisk. Together we can create life-changing innovation. Together we can make it...

Description : 1. MSL Strategic Synergy and Oversee • Guide the MSLs to develop regional medical plan based on competitor intelligence, academic needs, market situation and provincial policy to meet TA unmet regional needs, synergy into an overall MSL strategy in the national level. • Review the budget proposal from MSLs, co-work with TA head 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...

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...

ABOUT ABBOTT DIAGNOSTICS: The key to successful treatment and full recovery is often fast, accurate diagnosis. Abbott’s life-changing tests and diagnostic tools provide insights that enable smarter, faster decisions and transform the way the world is managing health. Our pioneering technology spans the world of healthcare operations — with medical...

Job DescriptionHead of Regulatory Affairs for GSK in China will provide leadership and strategic direction for the company's regulatory affairs team. The role involves ensuring the registration of new products and line extensions, managing the life cycle of products, and aligning with commercial and global regulatory objectives.About the RoleLead a team of...

Are you passionate about driving innovation in the pharmaceutical industry and transforming the treatment paradigm for chronic diseases? Novo Nordisk A/S, a leading international pharmaceutical company, is seeking an experienced Regulatory Affairs Supervisor to join its team.The ideal candidate will have a strong background in regulatory planning,...

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...

About the RoleThis is a challenging opportunity for an experienced MSL Manager to lead our regional medical strategy in Beijing. As a key member of our medical affairs team, you will be responsible for developing and implementing strategic plans to drive business growth and improve patient outcomes.

About the RoleWe are seeking a highly skilled Regulatory Affairs Manager to join our team at Takeda in Beijing. As a key member of our regulatory affairs team, you will be responsible for ensuring compliance with drug administration and registration management regulations.Key ResponsibilitiesDevelop and implement product registration plans, coordinating with...

Key responsibilities  重要职责 Develop regional medical strategy and ensure top level medical contribution to internal and external customers. Regional KOL management IIS Regional medical project Knowledge, skills and experience  知识、技能和经验 • Medical Master degree or above, preferable in endocrine or Cardiology. ...

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,...