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Principal/Associate Director, Physician (Immu-Cell Therapy)

地点 北京, 北京, 中国 上海, 上海, 中国 职位 ID R-187320 发布日期 12/18/2023

Responsible for providing technical leadership as compound or indication lead within a cross-functional team to design, execute, analyse and interpret clinical studies. Ensures projects (including multiple studies) adhere to Good Clinical Practice and regulatory requirements.

Typical Accountabilities

  • Provides expertise to China development strategy and plan for all portfolio projects within the own area of specialty.
  • Leads and/or performs China protocol development, preparation for clinical challenges and governance committee review, as well as health authority interactions.
  • Manages clinical trials as a medical lead to deliver study with cooperating with cross-functional partners.
  • Provides, as an expert, strategic physician expertise to quantify the benefits, risks, value and uncertainty of  clinical trials.
  • Ensures efficient and effective leadership and management of project information, strategy, quality standards, and integrity of information interpretation.
  • Networks with colleagues and experts, providing medical consultancy in own area of expertise and serving as a resource for others by sharing experience within and beyond project team.
  • Keeps close connection with global study team during the entire course of the study.
  • Coaches junior physicians and provides supervision as needed.
  • Keeps own knowledge of best practices and new relevant developments up to date.

Education, Qualifications, Skills and Experience

Essential

  • Master degree in medical discipline or above
  • Experience as a clinical physician
  • Experience of management and design of clinical trials
  • Minimum 7 years of experience as clinical research physician in pharma industry R&D .
  • Therapeutic area expertise

Desirable

  • PhD in scientific discipline
  • Extensive general medical knowledge
  • Extensive experience in managing or designing complex clinical trials which require close monitoring

【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。】



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 authorisation and employment eligibility verification requirements.

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