- 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.
- 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
- PhD in scientific discipline
- Extensive general medical knowledge
- Extensive experience in managing or designing complex clinical trials which require close monitoring
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AstraZeneca Jing'An, 中国 全职At AstraZeneca, we turn ideas into life changing medicines. Working here means being entrepreneurial, thinking big and working together to make the impossible a reality. We're passionate about the potential of science to address the unmet needs of patients around the world. We co ...
Assoicate Director, Physician, Lung Cancer - Jing'An, 中国 - AstraZeneca
描述
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
Essential
Desirable
Date Posted
26-3月-2024Closing Date
30-7月-2024