Typical Accountabilities:
- Takes medical responsibilities to ensures successful conduct and integrity of all in-scope clinical studies
- Work as China study physician in China-join global studies, PK studies or country-specific clinical initiatives under the supervision from program/study lead physicians.
- Contributes to study design and develops appropriate protocol synopsis and protocols/amendments to match China clinical practice and meet regulatory requirement.
- Provides medical monitoring for the trials to review medical data, evaluate AEs/SAEs and detect safety signals, to ensure the data with high quality and the safety of participants.
- Supports document preparations for China regulatory filing and registration as a TA clinical science expert.
- Provides consultation to clinical operation colleagues on protocol design questions and answering protocol related questions from site investigators as a clinical science physician.
- For China join global studies, keeps close connection with global study team during the entire course of the study.
- Responsible for interacting and communicating with China KOLs for China development plan and protocol design.
- Coaches junior colleagues and provides support as needed.
- Maintains up-to-date medical/scientific knowledge as well as clinical trial landscape and competitive intelligences in the TA.
- Other tasks assigned by line manager as appropriate.
Education, Qualifications, Skills and Experience:
Essential
- Master degree in medical discipline or above
- Experience of management and design of clinical trials;
- At lease 3 years of physician experience in drug development in pharmaceutical company.
Desirable
- PhD in scientific discipline
- Extensive general medical knowledge
- Extensive experience in managing or designing clinical trials
- Thorough knowledge of study analysis and design in all phases of drug development
Date Posted
14-7月-2026Closing Date
29-9月-2026AstraZeneca 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.
Skills Required
- Master degree in medical discipline or above
- Experience of management and design of clinical trials
- At least 3 years of physician experience in drug development in pharmaceutical company
- PhD in scientific discipline
- Extensive general medical knowledge
- Extensive experience in managing or designing clinical trials
- Thorough knowledge of study analysis and design in all phases of drug development
AstraZeneca Compensation & Benefits Highlights
The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about AstraZeneca and has not been reviewed or approved by AstraZeneca.
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Fair & Transparent Compensation — Pay is considered competitive across many roles when total rewards are factored in. Senior scientific and leadership bands are described with high ranges that reinforce competitiveness at upper levels.
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Strong & Reliable Incentives — Bonuses, equity eligibility in many salaried roles, and solid sales on‑target earnings with upside are emphasized as meaningful parts of compensation. These elements boost overall value even where base pay is not the very highest.
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Retirement Support — A 401(k) program with a strong company match and immediate vesting is repeatedly cited as a standout. Generous retirement support is viewed as enhancing the total package relative to peers.
AstraZeneca Insights
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