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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 The Clinical Research Associate (CRA) is responsible for managing and monitoring the conduct of clinical projects according to ICH-GCP, Standard Operating Procedures (SOP) and applicable Project Management Plan (PMP) and local regulatory requirements. Responsibilities: Contribute comments/input in the development of Protocol,...

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...

Description Clinical Research Associate (CRA) Job Description The Clinical Research Associate (CRA) is responsible for managing and monitoring the conduct of clinical projects according to ICH-GCP, Standard Operating Procedures (SOP), and applicable Project Management Plan (PMP) and local regulatory requirements. Responsibilities Job...

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...

When our values align, there's no limit to what we can achieve. At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.Each of us, no matter what we do at...

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...

When our values align, there's no limit to what we can achieve. At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.Each of us, no matter what we do at...

Welo Life Sciences, a Welo Global brand, is a specialized language and technology partner serving pharmaceutical, CRO, and medical device organizations operating in regulated global markets. We deliver regulator-ready translation, linguistic validation, and localization solutions that support clinical trials, pharmacovigilance, regulatory affairs, labeling,...

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...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionSummary of Essential Functions:Prepares, reviews and coordinates, under guidance, local regulatory submissions (MoH, EC, additional special national local applications if applicable, e.g. gene therapy approvals, viral safety dossiers, import license) in alignment with global...

该职位来源于猎聘 岗位职责： 1、策略与方案：制定临床开发策略（CDP），审核Ⅰ–Ⅲ 期方案、IB、ICF、CSR等关键文件、立项医学评估。 2、医学监查：主导 Ⅰ–Ⅲ 期临床开发，审批方案 /...

Serve as SDTL Responsible 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 quality Contributes in...

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;...

****Who We Are**** Emerald Clinical Trials is a **global leader** in clinical research, partnering with over **160 biotech** companies and **15 of the world’s top 20** pharmaceutical firms. Headquartered in Singapore, we combine scientific excellence with operational expertise to deliver end-to-end clinical trial solutions across all phases,...

****Who We Are**** Emerald Clinical Trials is a **global leader** in clinical research, partnering with over **160 biotech** companies and **15 of the world’s top 20** pharmaceutical firms. Headquartered in Singapore, we combine scientific excellence with operational expertise to deliver end-to-end clinical trial solutions across all phases,...

**Serve as SDTL** - Responsible 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 quality -...

Serve as SDTL * Responsible 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 quality *...

• 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 timelines.• Perform...