Clinical Research Jobs in Shanghai

Key Responsibilities: Provide education on all aspects of the device device handling implantation and troubleshooting techniques related to equipment tools and products required for device implants. Develop and continuously improve training curriculum training materials and training tools based on c...

Patients with mitral and tricuspid heart valve disease often have complex conditions with limited treatment options. Our Transcatheter Mitral and Tricuspid Therapies (TMTT) business unit is boldly pursuing an innovative portfolio of technologies to address a patients unmet clinical needs. Its our dr...

Were on a mission to change the future ofclinical research. At Perceptive we help thebiopharmaceutical industry bring medicaltreatments to the market faster.Our mission is to change the worldbut to do this we need people like you.Apart from job satisfaction we can offer you:YOURSELF Starting at 14 d...

At Medtronic you can begin a life-long career of exploration and innovation while helping champion healthcare access and equity for all. Youll lead with purpose breaking down barriers to innovation in a more connected compassionate world.A Day in the LifeResponsibilities may include the following an...

AbbVies mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on peoples lives across several key therapeutic areas immunology oncology neuroscience and eye c...

JLL empowers you to shape a brighter way.Our people at JLL are shaping the future of real estate for a better world by combining world class services advisory and technology for our clients. We are committed to hiring the best most talented people and empowering them to thrive grow meaningful career...

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...

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...

conducting the study(ies) and reporting study data as required by the study protocol applicable regulations and guidelines and sponsor requirements.Essential Functions Perform site monitoring visits (selection initiation monitoring and close-out visits) in accordance with contracted scope of work an...

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...

Job TitleAssociate Clinical Operations ManagerJob DescriptionPhilips is a global leader in health technology committed to improving billions of lives worldwide and striving to make the world healthier and more sustainable through innovation. Driven by the vision of a better tomorrow.But its not just...

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...

Job OverviewAssists with the design/development of software solutions requiring general domain knowledge and limited business expertise.Troubleshoots code issues and continuously evolves IQVIAs platforms to meet user requirements/needs.Essential Functions Assists with the design/development of softw...

Job Overview:Site monitoring and site management responsibility for clinical studies according to Company and/or Sponsor Standard Operating Procedures and Regulatory Guidelines. Assures the implementation of project plans as assigned.Summary of Responsibilities:Responsible for all aspects of study s...

Job Overview:The Senior CRA I is responsible for site monitoring and site management. Responsibility for clinical studies according to Fortrea and/or Sponsor Standard Operating Procedures and Regulatory Guidelines. The Senior CRA I assure the implementation of project plans as assigned. Function as...

Job Overview:The Senior CRA I is responsible for site monitoring and site management. Responsibility for clinical studies according to Fortrea and/or Sponsor Standard Operating Procedures and Regulatory Guidelines. The Senior CRA I assure the implementation of project plans as assigned. Function as...

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...

Job Overview:Manages ARC review and is responsible for performing TMF review of electronic Trial Master Files (eTMF) Trial Country and Site artifacts for clinical studies in support of sponsors services contracts and internal Fortrea business needs.Summary of Responsibilities:Position provides proce...

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...

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...