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Physician I / II

Местоположение Shanghai Downtown, Shanghai Shi, Китай Идентификатор вакансии R-100983 Дата публикации 02/22/2021

Description

Key Tasks

  • Work closely with physician scientist for China development strategy and plan (including protocols) for all portfolio projects

  • Work closely with physician scientist to ensure successful conduct and integrity of all in-scope clinical studies (i.e., providing medical monitoring)
  • Work closely with physician scientist to co-own of clinical study delivery (with Stats and Clinical Operations)
  • Work closely with physician scientist for development clinical documents (CIB, protocol and CSR, ETC)
  • Work closely with physician scientist to analysis and interpretation of clinical study results in partnership with BIS
  • Work closely with physician scientist to forming and running advisory board for portfolio projects; Be responsible for interacting and communicating with China KOLs for China development strategy and protocol design
  • Support protocol development preparation for review by the Clinical Challenge and Protocol Review Committee
  • Work closely with physician scientist to setting strategic direction for addressing medical issues in regulatory submission and communication/interaction
  • Supporting China regulatory filing and registration
  • Providing consultation to clinical operation colleagues on protocol design questions and answering protocol related questions from site investigators
  • Work closely with physician scientist to represent TA Clinical Science at China Product Team
  • Work closely with physician scientist to interface with GPT MSD/physicians on clinical sciences matters
  • Work closely with physician scientist to provide clinical science support to BD and AZ China projects on needed base

Essential

Academic / Professional Qualification

A graduate degree of clinical, biomedical, scientific degree with significant drug development experience is required

Technical / Skills Training

  • General therapeutic area/disease Knowledge
  • General compound knowledge
  • General Regulatory knowledge
  • Investigator & site knowledge
  • GCP knowledge
  • Basic Medical monitoring
  • Safety monitoring and evaluation of signals
  • CSP/CSR content & data analysis
  • Presentation & communication skill
  • Clinical trial landscape and competitive intelligences

Working Experience

1-2 years clinical drug development or medical affairs experience within a pharmaceutical company

【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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Отличная корпоративная культура, отличные рабочие условия, поддерживающий менеджмент. Возможность ротации внутри компании. Они ценят инклюзивность и разнообразие.