Clinical Trials Jobs in Shanghai

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionJoin Us as a Compilation Specialist - Make an Impact at the Forefront of InnovationThe Compilation Specialist provides complex study reporting and other project services to department personnel. Compiles coordinates revises...

Not just a job but a careerYokogawa award winner for Best Asset Monitoring Technology and Best Digital Twin Technology at the HP Awards is a leading provider of industrial automation test and measurement information systems and industrial services in several industries.Our aim is to shape a better f...

Work Flexibility: HybridPosition summary:Responsible for the day-to-day management of one or more clinical studies to include pre-market post-approval post-market surveillance feasibility and/or marketing studies and/or investigator initiated studies.Responsible for ensuring that assigned studies ar...

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...

200多年来阿克苏诺贝尔一直致力于开创无限可能向世界呈现面面精彩作为油漆和涂料领域的领航者我们的产品已经融入人们的工作和生活阿克苏诺贝尔旗下品牌阵容鼎盛拥有多乐士Dulux国际International新劲SikkensInterpon等著名品牌在全球广受信赖阿克苏诺贝尔致力于成为全球行业领导者足迹已遍及世界150多个国家与地区阿克苏诺...

Working with UsChallenging. Meaningful. Life-changing. Those arent 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 breakthrou...

Summary of Responsibilities:Site management responsibility for clinical studies according to Fortreas Standard Operating Procedures ICH GCP Guidelines applicable project plans and Sponsor requirements including verification of study training records.Conducts site monitoring responsibilities for clin...

Monitors activities conducted by clinical investigative sites as they relate to AbbVie clinical studies to ensure successful execution of the protocol. Ensures adherence to federal regulations and applicable local regulations Good Clinical Practices (GCPs) ICH Guidelines AbbVie Standard Operating Pr...

Job Description SummaryThis role will take lead for the east China region all market access projects for all business units.GE HealthCare is a leading global medical technology and digital solutions innovator. Our purpose is to create a world where healthcare has no limits. Unlock your ambition turn...

When our values align theres no limit to what we can achieve.At Parexel we all share the same goal - to improve the worlds 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...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionJoin Us as a Lead Medical Project CoordinatorAt Thermo Fisher Scientific youll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our custo...

Working with UsChallenging. Meaningful. Life-changing. Those arent 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 breakthrou...

We are looking for a senior professional to help us sell our clinical trial operations in Brazil to Chinese pharmaceutical companies connecting Chinese Pharma to Brazil.Key Responsibilities:1. Serve as the primary commercial lead and bridge between Chinese pharma R&D teams and our clinical trial pla...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob Descriptionrequest physician for Cell therapy. detailed JD is not availed now. pls refer to PPD MD JD:As part of the Thermo Fisher Scientific team youll discover meaningful work that makes a positive impact on a global scale. Join our...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionJoin Us as Associate Director Clinical Operations Make an Impact at the Forefront of InnovationWe have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs spanning 2700 clinical trials acro...

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...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionJoin Us as a Clinical Compliance Manager - Make an Impact at the Forefront of InnovationThe Clinical Compliance Manager is responsible for the assessment management and reporting of serious breaches of GCP and protocol in cl...

Essential Functions May act as a Project Manager for a large stand-alone programme involving several regulatory or technical deliverables and/or region and/or operation; Undertakes risk analysis management and contingency plans as appropriate; Provides strategic regulatory and/or technical consultan...

In cooperation with affiliate / Area Medical teams Marketing RA Clinical and other functional areas provides leadership oversight and support for assigned products/projects. Establishes and approves scientific methods for hypotheses rational design of affiliate/Area/Global protocols and their report...

At Gilead were creating a healthier world for all people. For more than 35 years weve tackled diseases such as HIV viral hepatitis COVID-19 and cancer working relentlessly to develop therapies that help improve lives and to ensure access to these therapies across the globe. We continue to fight aga...