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临床项目经理(香港项目经验)
3-6万
人 · 本科 · 5年及以上工作经验 · 性别不限2024/09/12发布
五险一金绩效奖金年终奖金弹性工作定期体检

广州市越秀区太和岗20号3号楼2楼

公司信息
圣方(上海)医药研发有限公司

民营/150-500人

该公司所有职位
职位描述
Elixir Clinical Research Co., Ltd. (ECR Global) is currently looking for a Senior Project Manager (SPM) / Associate Director, Project Management (PMAD) to lead global clinical research studies in the Asia Pacific region. ECR Global is a technology-enabled CRO involved in full services for our clients, giving the ECR Global project teams the empowerment to truly lead and execute clinical trials.
Responsibilities
The SPM/PMAD position performs project lead role for multiservice global clinical trials. The position interacts with sponsors and manages the timeline and project deliverables. This role coordinates for all services contracted for the study.
The SPM/PMAD is also responsible for lead cross functional team of clinical monitoring, study start-up, regulatory, contract, safety, medical monitoring etc. You may need to attend bid defense meetings and support business development team in winning new business.
Our full-service approach is led by medical, regulatory and operational experts with deep therapeutic experience. The disciplined processes, site relationships, and technologies enable you to execute even the most complex global studies. Therapeutic focus areas including oncology, cardiovascular, endocrine/metabolic, infectious disease, CNS. Trials include those in Advanced Therapies, e.g., cell and gene therapies.
Qualifications
· Bachelor’s degree in a health related field (Master’s degree above is preferred);
· At least three years of clinical trial management experience in Asia Pacific region ideally in a CRO environment;
· Excellent planning, organisation, prioritisation skills;
· Flexible, accountable and comfortable in working in a global environment;
· Fluent in English and business level in Mandarin.
ECR Global Overview
Elixir Clinical Research Co., Ltd. (ECR Global) is a global technology-enabled full service CRO, is committed to improving R&D efficiency and empowering post-marketing real-world studies based on digitalization and AI technology. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Shanghai, China, employing around 500 people. Our mission is to provide one-stop professional solutions covering the overall product lifecycle from R&D to commercialiazation for pharmaceutical and medical device companies and scientific research institutions worldwide, aiming to accelerate the launching process of new drugs and benefit patients worldwide.

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