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● 招聘公司：Covance
● 公司简介：Covance（科文斯）是全球最大、最全面的药物开发公司之一。公司以其综合服务能力著称，包括临床前毒理实验、中心实验室服务、完整的生物产品生产设施以及I-IV期临床试验管理和健康经济学等其他服务。● 招聘职位：肿瘤临床研究经理 ● 职位类型：全职 ● 职位薪酬：$90,000+ ● 工作内容：CRM负责执行和监督当地的临床试验操作活动，并在符合ICH GCP和国家法规的国家业务层面上对客户的当地监管和财务合规具有所有权、监督和影响。 ● Responsibilities：The CRM is accountable for execution and oversight of local operational clinical trial activities and has ownership, oversight and impact on local regulatory and financial compliance, at a country operations level at the client in compliance with ICH GCP and country regulations. ● 职位要求： - 大学/专科学位(生命科学优先)，或相关的专职医疗专业认证，护理认证，医学或实验室技术
- 申请人如有至少四(4)年或以上制药或制药行业的相关临床研究经验，或在医疗机构有相关工作经验，可获考虑
- 全面了解ICH准则和GCP，包括对其他国家监管要求的基本了解
- 深入了解药物开发过程
- 熟练使用当地办公语言和英语，包括书面和口头
- 良好的电脑操作技能，熟悉电脑操作
- 领导和发展初级员工的能力
- 灵活并能适应不断发展的工作环境
- 至少6-8年的临床研究经验
● Requirements： - University/college degree (life science preferred), or certification in a related allied health profession from an appropriately accredited institution, nursing certification, medical or laboratory technology
- In lieu of the above requirement, candidates with minimum of four (4) or more years of relevant clinical research experience in pharmaceutical or CRO industries or experience in a health care setting will be considered
- Thorough knowledge of ICH Guidelines and GCP including a basic understanding of regulatory requirements in other countries
- Thorough understanding of the drug development process
- Fluent in local office language and in English, both written and verbal
- Good computer skills with good working knowledge of a range of computer packages
- Ability to lead and develop junior staff
- Flexible and adaptable to a developing work environment
- Minimum of six-eight (6-8) years of clinical research experience
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