登录/注册我是招聘方 免费发布职位
临床项目经理（熟悉香港中心）
30-50K/月广东省-广州/本科及以上/5-10年
李菊一周前来过
圣方（上海）医药研发有限公司
职位详情
岗位职责
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.
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.
任职要求
无
相似职位
微信登录/注册
验证码登录/注册
公司信息
圣方（上海）医药研发有限公司
- 上海
- 无
- 医药辅料
- 民营
- 不需要融资
圣方（上海）医药研发有限公司，是一家科技型全功能临床CRO。秉承“让好药触手可及”的使命，圣方医药研发已为数百家制药企业提供高质效的临床研究解决方案，助力新药快速上市。
圣方医药研发的业务能力涵盖BE、I-IV期临床试验、真实世界研究以及最终的申报注册。通过在临床研究信息化运营管理的多年实践，和临床研究行业资源的开发与整合，圣方医药研发形成了独特的新型临床研究模式：以项目、文件、人员、数据、不良反应等信息化运营管理，为临床研究项目的高质量开展打下扎实基础；与临床研究机构、第三方合作伙伴以及监管机构的对接，链接临床研究各相关方，形成高效、透明、协同的项目运行机制；基于TrialOS平台的海量信息和强大精准的数据分析引擎，项目全程数据驱动，实现精准预测、风险防范、质量把控，大幅提升药物的研发质量和研究成果的产出效率。
圣方医药研发拥有一支经验丰富的专家团队，可在临床研究方案设计、医学策略、法规注册、中心管理、数据管理、生物统计等临床研究的重要环节为客户提供高质量的服务。
