Medical Affairs Effectiveness Lead

Job SummaryWe are seeking a highly skilled Medical Affairs Effectiveness professional to join our team at Pfizer. The successful candidate will be responsible for reviewing and managing external funding risk, working closely with internal teams to improve pre-approval processes and develop corporate risk strategies.Key ResponsibilitiesReview and manage...

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...

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 Purpose:The Head of Regulatory Affairs, China will provide strategic direction for the GSK China Regulatory Affairs team. The role will ensure the registration of new products and line extensions and manage the life cycle of the products in line with commercial and global regulatory objectives. The role will maintain strategic relationships with key...

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...

Job SummaryWe are seeking a highly skilled and experienced Medical Communications professional to lead our China Medical Communications function. As a key member of our Medical Affairs team, you will be responsible for developing and implementing medical content strategies to support our business objectives in China.Key ResponsibilitiesDevelop and implement...

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 CompanyBristol Myers Squibb is a cutting-edge biopharmaceutical company driven by a singular vision: transforming patients' lives through scienceTM.Salary and BenefitsWe offer a highly competitive salary ranging from $120,000 to $180,000 per annum, based on experience and qualifications. In addition to a comprehensive compensation package, you can...

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...

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...

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...

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 Regional Medical Advisor at Novo Nordisk, you will play a crucial role in developing and implementing regional medical strategies to drive business growth and improve patient outcomes.Key AccountabilitiesDevelop and execute regional medical plans to ensure top-level medical contribution to internal and external customers.Manage key...

Job SummaryWe are seeking a highly skilled Medical Strategy Lead to join our team in Beijing. As a Medical Strategy Lead, you will be responsible for developing and implementing regional medical plans to meet the needs of our customers.Key ResponsibilitiesDevelop and implement regional medical plans to meet the needs of our customersGuide and coach Medical...

Key Responsibilities:As a Regulatory Affairs Specialist at Abbott, you will be responsible for the registration of medical devices, IVDs, and/or drug products. This includes ensuring timely submission of applications for new product registration, variations of marketed products, and license renewals, in compliance with NMPA/CMDE requirements and internal...

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.

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 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...