Clinical Research Specialist Jobs in China

Job Overview:Lead writer independently responsible for the preparation of clinical study protocols and clinical study reports (CSRs) and other documents as needed for lower complexity studies. Provides support to more experienced writers with the preparation of clinical study protocols and CSRs and...

Title:Senior Medical Science Liaison--BeijingCompany:Ipsen (Beijing) Pharmaceutical Science and Technology Developpement Co. LtdAbout Ipsen:Ipsen is a mid-sized global biopharmaceutical company with a focus on transformative medicines in three therapeutic areas: Oncology Rare Disease and Neuroscienc...

Job DescriptionOverall job purpose:The MSL is a field-based medical professional whose primary responsibility is to engage in non-promotional peer-to-peer communication & provide medical/scientific information to SLs and KDMs based on cutting-edge scientific exchange and services oriented towards th...

DescriptionJob Responsibilities Prepare for report and proposal writing with actionable recommendations independentlyConduct presentation to clients with guidance from managerFully responsible for daily project managementLead project teams to provide professional and precise all-around serviceInstru...

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...

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...

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...

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...

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...

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...

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 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 DescriptionNeed cardiologist with CV specialty and experiences in hospital settings for at least 5 years.Industry or regulatory experiences would be a plus.JD:As part of the Thermo Fisher Scientific team youll discover meaningful work...

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 ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionJoin Us as a Senior Medical Writer - Make an Impact at the Forefront of InnovationThe Senior Medical Writer provides high-quality medical and scientific writing from planning and coordination through delivery of final drafts...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionJoin Us as a Principal Medical Writing - Make an Impact at the Forefront of InnovationAs a Principal Medical Writer you will serve as the primary author by writing and providing input on routine documents such as clinical st...