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该职位来源于猎聘 Be responsible of product performance evaluation (including but not limited to clinical, instrumental, consumer, sensory and PCO test etc.), implementation, monitoring for the development of new products and new claims needs of product, and play as work package leader role to manage the project from end to end for performance...

Business Support 该职位来源于猎聘 Key Responsibilities Any assigned responsibilities as below: • Development and update on contracts templates, negotiation tools, fallback documents, including company level NDA/CDA(for sponsor/client and vendor), sponsor contracts, partner contracts, vendor contracts. • Coordinate with all functions on winning...

该职位来源于猎聘...

该职位来源于猎聘 We are currently seeking a Clinical Project Manager based in Shanghai or Guangzhou / Foshan to join our medical and clinical team. This person will be responsible for ensuring project plans are executed according to planned quality, timelines and cost. He or she will oversee the daily operation of various development programs,...

该职位来源于猎聘 职责描述： Reporting To PM Director Position description: Responsible for the overall management of projects to ensure the adherence of the project to quality standards and the approved timeline and budget in the service agreements. Leads the project team and the internal/external communications and identifies suitable...

该职位来源于猎聘 职责描述： 1. 负责临床试验项目质量管理体系的建立、实施与持续改进，确保研究过程符合GCP、ICH-GCP及国家相关法规要求； 2. 制定并执行临床试验各阶段的质量监控计划，包括中心启动前审核、监查访视质量评估、数据核查及文件合规性审查； 3....

该职位来源于猎聘 At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking...

该职位来源于猎聘 岗位职责： 1.担任临床研究项目管理负责人，助力实现全球临床开发计划中设定的试验目标。 2.参与临床项目管理的各个方面，包括采购成本、时间、质量、安全、沟通、风险控制、供应商、利益相关者管理以及全球范围内的情景规划。...

该职位来源于猎聘 **【岗位目标】** 作为上市前临床医学团队的核心成员，负责公司在**肾病、代谢、CNS、肝病（药物性肝损）**...

Essential Functions• Under general supervision, serve as Single Point of Contact (SPOC) in assigned studies for investigative sites, Site Activation Manager (SAM), Project Management team, and other departments as necessary. Ensure adherence to standard operating procedures (SOPs), Work Instructions (WIs), quality of designated deliverables and project...

该职位来源于猎聘 岗位职责： 1、This position will be responsible for all aspects of clinical pharmacology and biopharmaceutics studies in China by close collaboration with global QCP. This individual will be able to take the project lead to generate study designs, protocols, review/proofreading and author reports and co-author primary and...

Job Overview:Site Navigators play a critical role in the comprehensive coordination of site-level activities throughout the start-up phase of a clinical study and potentially through closeout activities as required. Serving as the single point of contact for investigative sites, this role ensures smooth progression from feasibility and initial outreach...

Job OverviewUnder moderate supervision, executes the feasibility, site identification regulatory, start-up, and maintenance activities in accordance with regulations, SOPs, and project requirements  at the regional, or country level.Prepares and manages site documentation; reviews and negotiates site  documents and contracts with sites and sponsors;...

该职位来源于猎聘 Job Responsibilities • With supervision from mentor/line manager, develop the strategic clinical development strategy and clinical development plan for the compound responsible, provide medical expertise for regulatory affairs, provide medical guidance on the business plan, and lead in scientific data dissemination (leading and...

At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure...

DescriptionResponsibilitiesPerforming site evaluation, initiation, monitoring and close-out visits, plus maintaining appropriate documentation according to a project-specific monitoring plan, ICH-GCP, and applicable regulations.Supporting the development of a subject recruitment plan. Establishing regular lines of communication plus administering protocol...

Working with UsChallenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the...

Serve as SDTLResponsible for planning and leading the delivery of all components of a clinical study to time, cost, and quality from Study Specifications (SS) through study closeout activities and Clinical Study Report (CSR).Form a motivated and aligned study team that delivers the study results on or ahead of time and to high qualityContributes in steering...

Serve as SDTLResponsible for planning and leading the delivery of all components of a clinical study to time, cost, and quality from Study Specifications (SS) through study closeout activities and Clinical Study Report (CSR).Form a motivated and aligned study team that delivers the study results on or ahead of time and to high qualityContributes in steering...

Serve as SDTLResponsible for planning and leading the delivery of all components of a clinical study to time, cost, and quality from Study Specifications (SS) through study closeout activities and Clinical Study Report (CSR).Form a motivated and aligned study team that delivers the study results on or ahead of time and to high qualityContributes in steering...