(Associate) RA Manager, Beijing

By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’sPrivacy Noticeand Terms of Use. I further attest that all information I submit in my employment application is true to the best of my knowledge.

Job Description

Objective / Purpose:

• In accordance with the company’s product launch strategy, lead and coordinate the process of drug registration and ensure the compliance of technical documentation and process to guarantee the success of drug registration.
• Complete related registration work of established product during the registration cycle to ensure the continuous effectiveness of Import Drug License.

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.
• May support or act as China regulatory lead (CRL) for assigned product/program, contributing to corresponding China Asia Development Team (CADL) and GRT (Global Regulatory Team) for regulatory related strategy, technical, planning input, etc.
• 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.
• Other assignments by line manager.

Qualifications & Skills:

• Level of Education: Bachelor’s degree or above majored in medicine or pharmacy.
• Working Experience in Relevant Field: >3 years 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. Teamwork and collaboration.

Locations

CHN - Beijing - Research and Development

Worker Type

Employee

Worker Sub-Type

Regular

Time Type

Full time