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您是否对新型的治疗型研发充满了热爱和希望，您是否对癌症的攻克和治疗的充满了信心和勇气，您是否对人类疾病治疗的探索充满了信念和执着，我们随时欢迎与我们有着共同愿景和美好愿望的您加入我们，让我们一起携手同行，致力于改善癌症患者的生活，共创美好！
我们的协作团队拥有深厚的科学、临床、业务知识和领导能力，我们诚邀您加入z-alpha！我们需要一支由拥有多样化思想、技能、经验和富有激情的人才组成的强大团队来助力诊断和治疗用途放射性药物产品的开发，为癌症患者带来新的机遇，焕发生命光彩。
09-13
高级科学家/副总监
——
SENIOR SCIENTIST/ASSOCIATE DIRECTOR, ONCOLOGY
09-13
临床药理高级科学家
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SR. SCIENTIST,CLINICAL PHARMACOLOGY
09-13
药物警戒医师
PV PHYSICIAN
09-13
质量保证总监
QA DIRECTOR
临床药理高级科学家
SR. SCIENTIST,CLINICAL PHARMACOLOGY临床药理高级科学家- CLINICAL SCIENCE
岗位职责：
● 在项目开发团队中代表临床药理学,并支持临床研究的临床药理学相关部分，包括方案设计、研究实施、数据分析、报告撰写和监管文件提交等
● 协调和监督临床药理学数据,确保所有执行符合部门]的战略，符合监管和法律要求，以及公司的标准操作程序
● 进行药代动力学(PK)药效学(PD)和剂量-暴露反应分析，以支持剂量选择、试验设计、内部决策、监管提交文件和发表文章
● 为临床前阶段项目提供意见，以优化体外和临床前数据，支持项目推进临床开发和提交新药申请
● 临床药理相关文档的撰写，中英语的口头交流、报告等
任职要求：
● 硕士及以上(博士优先)
● 药学、药代动力学、临床药理学、定量药理学、生物医学工程或相关领域;在制药企业或CRO公司有3年以上临床药理相关工作经验
● 熟悉临床药理学的法规要求和指南
● 熟练使用药代动力学软件(如Phoenix WinNonlin)，具有PKPD建模和仿真软件(如NONMEM、 R等)知识和技能是一-个加分项
● 良好的项目管理技能，以及与其他部门合作和管理与内部和外部合作伙伴的能力
● 英文良好，能够进行日常商务沟通
质量保证总监- QA
【视觉设计师】
岗位职责：
● Work on the Quality Management System setup / maintenance to ensure GCP processes / activities in compliance with applicable ICH guidelines and country regional regulations, in accordance with the company strategies
● Work with development team to support on clinical projects and ensure the quality on the processes / activities of document management, personnel qualification & training, management of GCP quality risks / issues, vendor management and strategy, audit plan, implantation and trend analysis, inspection readiness, continuous improvement
● Conduct audits as required
● Maintain a close and collaborative relationship with business functions to support quality needs
● Interact with regulatory inspection agencies, stay abreast of evolving regulations and influence future regulations, if applicable
任职要求：
● Bachelor or higher degrees (life science preferred, including medicine, nursing, biology and laboratory technology)
● 5 years or above in GCP quality in the biotech /pharmaceutical /CRO industry or the relevant clinical research field
● A broad understanding of drug research and development process, current knowledge of all applicable regulations governing the conduct of R&D pharma as well as a current knowledge of GxP are essential
● Good interpersonal skills, including but not limited to leadership, negotiation in difficult situations, handing multi-tasks are essential
● Fluent in written and verbal English
*请将您的简历发送到: zenterash@zenteratx.com
药物警戒医师
PV PHYSICIAN药物警戒医师- CLINICAL SCIENCE
岗位职责：
● Accountable and responsible for the medical review, analysis and approval of all individual Serious Adverse Event and Serious Adverse Reaction reports
● Provide guidance during the case handling and reporting cycle
● Determine seriousness, causality, and summarize Sponsor position for single case reports
● Perform analysis of similar events
● Lead the preparation of aggregate safety reports (DSURs), case narratives and any other safety medical documentation thus contributing to high quality standard documents within the organization
● Carry out continuous efficient evaluation of adverse event and all other safety information to predict and manage the safety profile of compounds in clinical development through identifying the need for updates to the reference safety information and drive proactive implementation of risk management initiatives in accordance with global regulatory requirements
● Provide medical guidance and training to team members
● Provide medical advice and support for the Pharmacovigilance component of feasibility studies
● Inform the appropriate team members of any new SUSAR or medically significant new information that might impact on the safety profile of the medicine
● Maintain knowledge and understanding of safety related regulations and guidelines
● Perform other duties as assigned
任职要求：
● Medical Degree from an accredited institution of Medical Education
● Minimum of 3 years clinical research or industry experience with at least 2 years of experience serving as a PV Physician
● Equivalent combination of relevant education and experience
● Good written and verbal communication skills
● Good organization skills and attention to detail
● Demonstrated ability to handle multiple competing priorities while adhering to applicable timelines
● Ability to work independently, prioritize work effectively and work successfully in matrix team environment
● Fluent in written and verbal English
*请将您的简历发送到: zenterash@zenteratx.com
高级科学家/副总监，肿瘤
SENIOR SCIENTIST/ASSOCIATE DIRECTOR, ONCOLOGY高级科学家/副总监，肿瘤- TRANSLATIONAL MEDICINE
岗位职责：
● Lead the scientific discovery and preclinical development of next generation immunotherapies
● Design and execute in vitro & in vivo studies in collaboration with external vendors
● Manage the program and present program data/update internally and externally
● Opportunity to explore on CMC development, analytical development, and IND submission
● Collaborate with translational research team and clinical development team to pursue the most promising clinical candidate
● Regular literature review and landscape analysis
● Participate in BD evaluation activities
任职要求：
● Ph.D. in cancer biology, molecular biology, immune-oncology or related fields with 3+ years of industry experience
● Deep understanding in tumor biology and technical expertise in antibody-based drug discovery and development
● Ability to independently design experiments, interpret results and strong problem-solving skills
● Project lead experience in pharmaceutical companies or expertise in protein engineering will be a plus
● Scientifically self- motivated and excellent research capabilities
● Leadership spirit and great communication skills, with proficiency in both spoken and written English
*请将您的简历发送到: zenterash@zenteratx.com
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