(Associate) RA Manager, Beijing
Beijing, Beijing Municipality- Job Type: Full Time
- Job Level: Senior
- Travel: Minimal (if any)
Global Regulatory Affairs (GRA) develops and executes innovative regulatory strategies to provide life-changing therapies to patients. GRA has a strategic role in all stages of global product development and across the Takeda Enterprise.
At Takeda, we strive to provide transformational opportunities for every member of our team, and we empower our people to take charge of their futures. In an environment that fosters lifelong learning and a growth mindset, you’ll have the support you need to thrive — at work and beyond.
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Job Description
Accountabilities:
- In accordance with the company’s product launch strategy and department’s work plan, take full responsibility of the product registration and application for approval and develop the plan by stage. Contribute to decision making on drug registration leading to minimal registration timeline.
- Guide subordinates to solve the problems occurred during drug registration in uncertainty Chinese pharmaceutical environment to achieve drug registration approvals in timely and cost-effective way.
- Summarize product registration related materials with coordination among head office, factory, Sales & Marketing. Provide corresponding support for the sales in China market.
- In accordance with the plan of product registration and application for approval, manage the necessary materials and information during the process and track and summarize the progress.
- Be responsible for submission of complete and qualified product application data to drug regulatory authorities, coordination of raw data review and on-site assessment.
- Manage and archive examination and registration materials and other relevant documents.
- Provide necessary support to the preparation and implementation of clinical trial.
- Establish influential relationships with key regulatory authority individuals and KOLs in relevant fields, such as SFDA, CDE, NIFDC, PIDC etc. Monitor regulatory environment and collect important information such as regulations, guidelines, competitive products etc.
- Establish and maintain internal/external channels of communication.
- Ensure regulatory activity is in compliance with authority and Takeda policy.
- Coordinate with the establishment of internal SOP and system.
Qualifications & Skills:
- Level of Education: Bachelor’s degree or above majored in medicine or pharmacy.
- Working Experience in Relevant Field: >5-year related work experience
- Professional Knowledge and Skills: Skilled in using computer office software. Good English or Japanese in listening, speaking, reading and writing. Be familiar with the laws and regulations of drug administration and registration management, stronger professional competency, excellent communication skill and leadership.
Locations
CHN - Beijing - Research and DevelopmentWorker Type
EmployeeWorker Sub-Type
RegularTime Type
Full timeThe heart of our work
Shining a light on new perspectives
Our pipeline
Our internal research capabilities and external partnerships contribute to an R&D engine that has produced exciting new molecular entities (NMEs) across our core Therapeutic Areas. Check out our pipeline and see how we’ll continue delivering a steady stream of next-generation therapies.
Working at Takeda
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Empowerment
Through trust and respect, you will have genuine support from leaders, managers, and colleagues to do your best work.
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Patient
Responsibly translate science into highly innovative medicines and accelerate access to improve lives worldwide.
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