Hiring.Camp

Senior Manager, Regulatory Project Management and Excellence,GRA China

Takeda

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Location
CHN - Beijing - Research and Development, China
Workplace
Hybrid
Type
Full-time
Department
Legal
Seniority
Manager
Experience
7+ years
Education
PhD
Source
Workday

Description

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Job Description




Job Description                                                                                                   

Job Title:

RA Senior Manager of Regulatory Project Management and Excellence

BU/Organization:

R&D

Department/
Function:

GRA

Location and Flex Work Arrangement:

Beijing or Shanghai; Hybrid

 

 

Job Code/
Job Profile:
not required for contractor

 

CHN R&D - Senior Manager, Regulatory Project Management and Excellence

Supervisor:

Zhizhong Duan

RA Operations Head

 

Compensation Grade Profile:
not required for contractor

 


CHN - TDC - Regional Grade F - Premium

 

 

Objective / Purpose:

  • Provide insights into initiative, strategy and activity to facilitate effective and excellent project operations.
  • Keep close contact with local and global stakeholders and cooperate with GRA operation and compliance.
  • Establish and ensure effective working models with internal stakeholders (global, regional, TDC, local commercial, etc.) and build the culture of partnership.
  • Project specific input for execution excellence.

Accountabilities:     

1.       Building up RA operations in-house team capability development according to external and internal.

  • Nurture innovation and solving problems creatively, commitment to excellence.
  • Analyze industrial practice and find out the areas which need to be improved and provide solutions.
  • Support the establishment and assessment of regulatory affairs capability and development scheme.
  • Streamline the working model for regulatory affairs team through the comprehensive understanding of the model of collaboration functions.
  • Organize/lead discussion on high frequency questions/issues and generate action plans.
  • Provide insights into the RA function daily work and work out the improvement plan if needed.
  • Assigned tasks including publishing and others.                                                                                                                                                                                

Education & Competencies (Technical and Behavioral):

·       Level of Education: Bachelor’s degree or above; Clinical medicine, life science (e.g. Chemistry, Pharmaceutics, Biochemistry, Biotechnology, Biology) or equivalent.

·       Working Experience in Relevant Field: Over 7 years’ experience in pharmaceutical industry or consultant firm over watching pharmaceutical industry, RA knowledge is preferred. Strategic thinking and big picture orientation.

·       Professional Knowledge and Skills: Familiar with the pharmaceutical products related policy, law and regulations; Have sense of pharmaceutical industry competitive landscape; Excellent communication skills in Chinese and English, both verbal and written; Expert in handling MS office (word, excel, PowerPoint etc.)

·       Desired education qualifications and equivalencies (e.g., PhD degree in a scientific discipline with 6+ years’ experience, or MS with 10+ years’ experience, or BS with 12+ years’ experience

 


 

Locations

Beijing, China

Worker Type

Employee

Worker Sub-Type

Regular

Time Type

Full time

Skills

ComplianceProject Management

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