When our values align, there's no limit to what we can achieve. Job Description: (Vaccine Project Team)Responsibilities: Oversee the registration process for the company's products, including but not limited to: Receiving, reviewing, and following up on registration applications to ensure all applications are submitted and processed on time; Communicating with product managers and technical support teams to ensure registration issues are resolved promptly; Organizing and archiving registration documents for easy traceability and management; Maintaining and optimizing the operation of the registration system to ensure its stability and reliability; Participating in discussions and implementation of new features and improvements to enhance the efficiency and user experience of the registration process.
Key Duties: Proficiently understand the registration processes and requirements of the company's products, ensuring comprehension of the company's registration policies; Possess strong communication skills and a team spirit, capable of effectively communicating with product managers and technical support teams to collaboratively solve problems; Have a solid foundation in data structures and basic programming skills to organize and archive registration data; Possess good English reading and writing abilities to read and understand relevant technical documents and registration requirements; Have an in-depth understanding of the product registration process and requirements, capable of identifying and resolving issues that arise during registration.
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Regulatory Affairs Manager - Fsp, Beijing
Free
Regulatory Affairs Manager - Fsp, Beijing
China, 北京, 北京,
发表 January 10, 2025
描述
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雇主信息
PAREXEL International is a leading global biopharmaceutical services provider, which continues to be a premier, trusted partner to clients who rely on the Company for expertise and flexibility, as well as the efficiencies of a worldwide infrastructure, to help them more quickly achieve their development and commercialization goals. For 30 years, PAREXEL has complemented client organizations with strategic insight, deep scientific knowledge, tactical expertise, and a wealth of experience throughout the development process. The Company's offerings include worldwide regulatory expertise, Phase I-IV clinical research services, eClinical technologies that accelerate development, and integrated commercialization services. PAREXEL is focused on providing tailored solutions that match a client's specific needs by applying the right blend of resources and capabilities, as well as the right guidance and high level of quality needed to help them bring safe and effective treatments to patients sooner.
Headquartered near Boston, Massachusetts, PAREXEL operates in over 70 locations throughout more than 50 countries, and has over 11,000 employees worldwide.
Visit www.PAREXEL.com for more information.
Specialties
Regulatory and product development consulting,
early phase clinical research,
phase II-III clinical research,
late phase clinical research,
eClinical solutions,
patient and site recruitment,
clinical logistics,
flexible outsourcing models,
strategic partnering