(Associate) Medical Affairs Manager

The Position Job Summary : Lead medical scientific affairs function, ensure its management of the affiliate adhering to the highest scientific and ethical standards and fulfilling all regulatory requirements. This position provides strategic directions and contributes to the collective medical management of the company and to the appropriate...

Job Description Summary Are you passionate about Regulatory Affairs? Would you love to work for a global organization that is “Doing More Good” for people and planet? Joining science and creativity, we are an international collective of thinkers who partner with customers to bring scents, tastes, experiences, ingredients, healthy and...

We’re looking for people who are determined to make life better for people around the world. The Associate Director of Corporate Affairs (CA) for Alzheimer's disease will play a crucial role in supporting both the development and implementation of international strategies to improve the detection, diagnosis, and care of Alzheimer's disease. Through a...

At Abbott, we believe people with diabetes should have the freedom to enjoy active lives. That’s why we’re focused on helping people with diabetes manage their health more effectively and comfortably, with life-changing products that provide accurate data to drive better-informed decisions. We’re revolutionizing the way people monitor their glucose...

About UsIQVIA is The Human Data Science Company, focused on using data and science to help healthcare clients find better solutions for their patients. With a strong commitment to innovation, we aim to harness advances in healthcare information, technology, analytics and human ingenuity to drive healthcare forward.Our MissionWe strive to empower our clients...

Description : Hydrafacial is hiring a Sr. Manager, International Regulatory Affairs, who is a key contributor in bringing the company’s products into new markets and spearheading global medical device/cosmetic regulatory submissions. Serves as the internal subject matter expert for international regulatory affairs on assigned projects/regions,...

Careers that Change Lives A Day in the Life Responsibilities may include the following and other duties may be assigned. Maintains a deep understanding of the science behind our products. Develops competitive intelligence in our product space. Drives education and outreach for safe and effective use of our products. Develops, implements and...

Join us on our exciting journey! IQVIA™ is The Human Data Science Company™, focused on using data and science to help healthcare clients find better solutions for their patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness advances in healthcare information, technology, analytics and...

Your Job The GPA (Government and Public Affairs) Specialist plays a critical role in supporting INVISTA’s government and public affairs initiatives. The specialist will be responsible for managing relationships with government officials, implementing government relations strategies, developing and executing public affairs strategies, managing...

The Position Main Tasks & Responsibilities 1. Facilitate the manager to make on mid- and long- term medical strategies and, after aligning with BA, implement them on yearly basis. 2. Work with line manager and BA to identify medical and scientific knowledge gaps and provide corresponding disease area medical messages. 3. Review and ensure...

Directly supporting EM MD and DVP China functionally on daily basis, the Medical Affairs Director will lead the strategies and goals for medico marketing activities across China, ensuring compliance with all applicable Company policies and industry standards in the affiliate. The incumbent will provide scientific and medical liaison to the DVP China. ...

Joinus in pioneering breakthroughs in healthcare. For everyone. Everywhere.Sustainably. Ourinspiring and caring environment forms a global community that celebratesdiversity and individuality. We encourage you to step beyond your comfort zone,offering resources and flexibility to foster your professional and personalgrowth, all while valuing your unique...

3M has a long-standing reputation as a company committed to innovation. We provide the freedom to explore and encourage curiosity and creativity. We gain new insight from diverse thinking, and take risks on new ideas. Here, you can apply your talent in bold ways that matter. Job Description: The Impact You’ll Make in this Role As a Regulatory Affairs...

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 Cardiology.  Fluent in...

The Position Principle Roles & Responsibilities / Accountabilities  • Provide medical perspective on the relevant brand(s) under the leadership of (Associate) Medical Director to ensure high-quality medical deliverables Periodically update medical plan/biomarker plan to reflect the change of the competitive landscape and critical business strategy...

Overview Post Date May 10, Number WEBCN-- Job Function Other Location 上海 Country Mainland China About the Position Responsibilities : • Builds and maintains smooth communication channels with local government departments (provincial Healthcare Security Administration and Health Commission etc.) and associations in relevant fields. •...

At Bayer we’re visionaries, driven to solve the world’s toughest challenges and striving for a world where ,Health for all, Hunger for none’ is no longer a dream, but a real possibility. We’re doing it with energy, curiosity and sheer dedication, always learning from unique perspectives of those around us, expanding our thinking, growing our...

Major Responsibilities/Activities: Provide regulatory input to supervisor for decision making on registration filing strategies. Set up product registration timeline and ensure well implement. Prepare and validate registration dossier to ensure fully meet Chinese regulations and guildlines. Track on-going projects and handle technical issues from...

EXPERIENCE: Over 5 years working experience in regulatory affairs for pharmaceuticals including more than 3 years in the project management post; Solid registration project management skills; Effective problem solving and planning capabilities; Good knowledge of CFDA regulations and guidelines; Good working relationship with regulatory authorities; ...

Job Overview: The Senior Medical and Regulatory Writer works independently to prepare and deliver clinical and regulatory documents for a wide range of therapeutic areas, performing the tasks listed below. Job Duties and Responsibilities: Write, edit, format, compile and review assigned documents requested by internal cross-functional teams and/or...