Senior/Principal/Associate Director, Statistician (Cell-Therapy)

OB REQUIREMENTS

Academic / Professional Qualification

• MSc/PhD in Statistics, Mathematics, or other related data science majors

• Knowledge of the technical and regulatory requirements related to the role

• Experience of regulatory interactions and/or submissions

Technical / Skills Training

• Excellent communication skills and ability to build strong relationships

• Collaborative - has the energy to work with R&D China & Global & across functional boundaries both internally and externally

• Ability to apply statistical expertise to complex problems, problem solving and quality focus

Working Experience

• Minimum 5 years of industry experience

• Leadership skill to lead and direct elements of project work

• Accountable for the statistical work

Duties & Responsibilities

• To lead the strategic and operation planning of the statistical contributions to the Development Plans, Regulatory Strategy and Submissions, Health Technology Assessment and Commercial support of AZ products.

• Leadership on the product so that all work is carried out with regards to AZ standards and external regulations

* Developing design options and providing high quality decision support

* Quantifying the benefit, risk, value and uncertainty of the emerging

product profile.

* Setting the standards (and enforcing compliance) for statistical work

within the product

• Holding CRO/Partners accountable for the high quality standards of their deliverables

• Represent AZ and Statistics to Health Authorities and Reimbursement/Payer Organizations for specific projects/indications

• Investigate and implement statistical approaches, for relevant statistical issues and/or regulatory guidance and/or value demonstration.

• Maintains understanding and awareness on new methodologies, therapy area and Development initiatives

• Provide leadership and direction to improvement projects/activities/initiatives and drive the implementation of best practice across the group

• Develops contacts with international opinion leaders, consultants and collaborative groups

• Ensure drug projects are successfully delivered in terms of scientific leadership and resourcing

【AstraZeneca is an equal opportunity employer. AstraZeneca will consider all qualified applicants for employment without discrimination on grounds of disability, sex or sexual orientation, pregnancy or maternity leave status, race or national or ethnic origin, age, religion or belief, gender identity or re-assignment, marital or civil partnership status, protected veteran status (if applicable) or any other characteristic protected by law. AstraZeneca only employs individuals with the right to work in the country/ies where the role is advertised.

阿斯利康是一家提供平等机会的企业，我们将考虑所有符合条件的求职者就业。不因残疾、性别或性取向、怀孕或产假状况、种族或民族或族裔出身、年龄、宗教或信仰、性别认同或变更、婚姻或伴侣关系、受保护的退伍军人身份（如果适用）及任何其他受法律保护的特征而产生歧视。】

Date Posted

15-9月-2026

Closing Date

29-11月-2026

AstraZeneca embraces diversity and equality of opportunity.  We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills.  We believe that the more inclusive we are, the better our work will be.  We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics.  We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements.