必需条件：   1.教育背景：已获得公共卫生政策与管理、社会医学与卫生事业管理、药物政策与药事管理、卫生经济学、医疗保障、监管科学等相关专业的博士学位。 2.研究能力：具备扎实的独立研究能力，精通政策分析、文献综述及定量/定性研究方法。拥有独立撰写并成功递交省部级及以上级别课题申请书（如国家自科、国家社科）的完整经验。 3.专业知识：深刻理解中国药品医疗器械监管体系、医疗卫生服务体系及生物医药产业政策框架。具备优秀的中英文书面写作与口头沟通能力。 4.个人特质：拥有出色的逻辑思维能力、战略洞察力、强大的自驱力与项目执行力，以及优秀的跨部门协同和对外沟通能力。 优先条件：   1.复合背景：拥有药学、临床医学或生命科学教育背景，并与上述政策管理专业结合的复合型博士人才；或具有海外顶尖公共卫生学院、药学院学习研究经历。 2.实践经验：拥有在政府研究机构、高端智库、国家级药械监管相关单位或国际组织从事政策研究的全职工作经验；或作为核心成员深度参与过国家级相关领域的重大战略课题研究。 3.领域专长：熟悉粤港澳大湾区政策环境，对真实世界证据（RWE）应用于监管决策、健康技术评估（HTA）、医保支付改革等专题有深入研究。能熟练使用Stata、R、Python等至少一种数据分析软件进行政策评估研究。

Qualifications: Mandatory Requirements:   1.Education: A conferred Ph.D. in Public Health Policy and Management, Social Medicine and Health Services Management, Drug Policy and Pharmacy Administration, Health Economics, Medical Insurance/Healthcare Security, Regulatory Science, or closely related fields. 2. Research Proficiency: Demonstrated strong independent research capabilities, with expertise in policy analysis, literature review, and quantitative/qualitative research methods. Demonstrated experience in independently drafting and successfully submitting competitive research proposals at the provincial/ministerial level or above (e.g., NSFC, NSSFC). 3. Domain Knowledge: Deep understanding of China's drug and medical device regulatory system, healthcare service system, and biopharmaceutical industry policy framework. Excellent written and verbal communication skills in both Chinese and English. 4.Personal Attributes: Outstanding logical thinking, strategic acumen, strong self-motivation, project execution ability, and excellent skills in cross-departmental collaboration and external communication. Preferred Qualifications:   1.Interdisciplinary Background: A combined academic background in Pharmacy, Clinical Medicine, or Life Sciences with the aforementioned policy/management disciplines; or research experience from top-tier overseas schools of public health or pharmacy. 2.Practical Experience: Full-time work experience in policy research at government think tanks, high-end advisory bodies, national-level drug/device regulatory agencies, or international organizations; or core participation in major national-level strategic research projects in relevant fields. 3.Specialized Expertise: Familiarity with the Greater Bay Area policy environment. In-depth knowledge of real-world evidence (RWE) for regulatory decision-making, health technology assessment (HTA), or healthcare payment reform. Proficiency in using at least one data analysis software (e.g., Stata, R, Python) for policy evaluation research.

1.政策追踪与分析：持续跟踪、研判国内外（重点聚焦粤港澳大湾区）在药品医疗器械监管、临床试验管理、真实世界研究应用、生物医药产业发展等领域的前沿政策、法规动态与发展趋势，形成前瞻性分析报告。 2.研究项目全周期管理：独立或作为项目核心人员，承接并高质量完成各级政府、监管机构委托的各类“软课题”研究项目（如监管科学、产业政策、卫生经济学评价等），包括课题设计、申请、执行与结题。 3.科研项目申请与执行：主动策划、撰写并申请国家自然科学基金、国家社科基金及省市级科技计划等相关领域的纵向科研项目，主导或参与项目实施。 4.成果转化与决策支持：将研究成果有效转化为高质量的内参报告、政策建议、规划方案或标准草案，为中心与政府部门的沟通洽谈及核心战略规划提供扎实的研究支撑与决策依据。 5.跨部门协同与知识传播：与内部科研、临床、运营团队紧密协作，对外与学术界、产业界及政策制定机构建立并维护良好的研究合作关系，传播中心的研究观点与影响力。

Key Responsibilities: 1. Policy Monitoring & Analysis: Continuously monitor, analyze, and assess domestic and international policy, regulatory developments (with a focus on the Greater Bay Area) in areas such as drug and medical device regulation, clinical trial administration, real-world study application, and biopharmaceutical industry development, producing forward-looking analytical and policy research reports. 2. Full-cycle Research Project Management: Independently or as a core lead, undertake and deliver high-quality “soft science” research projects commissioned by government authorities and regulatory agencies (e.g., regulatory science, industrial policy, health economics evaluation), encompassing project design, proposal writing, project implementation, and final deliverables. 3. Grant Acquisition & Execution: Proactively conceptualize, write, and apply for national and subnational research funding programs, such as those from the National Natural Science Foundation of China (NSFC), National Social Science Fund of China (NSSFC), and provincial/municipal science and technology programs. Lead or participate in project implementation. 4. Knowledge Translation & Decision Support: Effectively translate research findings into high-quality internal policy briefs, policy recommendations, planning proposals, or draft standards, providing robust research-based support and evidence for BAY TRIAL's communications with government entities and its core strategic planning. 5. Cross-functional Collaboration & Knowledge Outreach:  Collaborate closely with internal scientific, clinical, and operational teams. Build and maintain productive research partnerships with external academic, industry, and policy-making institutions to disseminate BAY TRIAL's research perspectives and influence.

职位概述： 粤港澳大湾区国际临床试验中心（BAY TRIAL）作为服务国家战略的核心创新平台，现诚聘一位具有战略视野与独立研究能力的政策研究专家。本职位旨在为中心构建专业的智库功能，将作为关键智囊，系统开展与药械监管创新、产业生态发展及跨境协同机制等相关的政策研究，将深刻洞察转化为推动行业发展的前沿思想与可行方案，直接赋能中心与区域的战略决策。

Position Overview: The Greater Bay Area International Clinical Trials Center (BAY TRIAL), a core innovation platform serving national strategies, is seeking a highly qualified policy research professional with strong strategic vision and independent research capabilities. This role is pivotal in establishing an in-house think tank function. You will serve as a key intellectual contributor, conducting systematic policy research on pharmaceutical and medical device regulatory innovation, industry ecosystem development, and cross-border collaboration mechanisms. High-quality research insights will be translated into forward-looking perspectives and actionable policy solutions that directly inform and empower the strategic decision-making of BAY TRIAL and the region.

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