Clinical Trials Jobs in Beijing

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 responsibi More...

Job Descriptionresponsible for study initation and clinical study conductionresponsible for clinical development plan execution and owner of clinical studies in dedicated disease areaThis individual will serve as the key interface between headquarter project development team and China More...

Job DescriptionPosition title: Manager CMC Regulatory AffairsDepartment: Regulatory AffairsReport to: Associate Director of CMCLocation: Beijing/Shanghai ChinaResponsibilitiesTake CMC lead for products under clinical development and for marketed drug products. Coordinate various aspec More...

Are you looking for a role where you can showcase your process improvement skills If so this is the job for you.As Regulatory Affairs Management Professional you will be responsible for leading a process improvement effort across the organization focusing on business alignment cost an More...

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 dee More...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionAt 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 customers to make the world healthi More...

Job Description SummaryThe Sr. Research Manager is responsible for defining strategy and overseeing the execution of academic research partnerships in China. This individual provides the interface between business segment region leaders and strategic collaborative academic partners More...

JOB DESCRIPTION:KOL management Responsible for identification/mapping and managing Key Opinion Leaders in defined TA in assigned cities. Develop scientifically based peer-to-peer relationships with KOLs through scientific exchange and value co-created medical activities. Identify an More...

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 dee More...

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 responsibi More...

At Alcon we are driven by the meaningful work we do to help people see brilliantly. We innovate boldly champion progress and act with speed as the global leader in eye care. Here youll be recognized for your commitment and contributions and see your career like never before. Together More...

Job DescriptionOverviewDirector of Monitoring Excellence is a member of the Monitoring Excellence Team reporting to the Global Head of Monitoring Excellence.Works in close collaboration with the Head of the Regions GCTO Leadership Team PSRM Research Procurement Functional Service Prov More...

Job Overview:Primary contact with investigative sites during study maintenance and -when assigned- site startup activities with responsibility for collection of the required investigator and regulatory essential documents to ensure EC/IRB/Third body/Regulatory Authority submissions ar More...

Job DescriptionThe CTA is an administrative support role for clinical trials. The role responsibilities include but not limited to the following activities:Basically Safety reports distribution and tracking. TMF support for country level document uploading to eTMF assist with eTMF rec More...

Job OverviewAssemble laboratory test kits for use by investigators to collect data on clinical trials participants.Work performed is in accordance with ICH E6 Guideline for Good Clinical Practice.Essential Functions Assemble test kits with specimen collection materials as per protocol More...

Job OverviewAssemble laboratory test kits for use by investigators to collect data on clinical trials participants.Work performed is in accordance with ICH E6 Guideline for Good Clinical Practice.Essential Functions Assemble test kits with specimen collection materials as per protocol More...

Job OverviewAssemble laboratory test kits for use by investigators to collect data on clinical trials participants.Work performed is in accordance with ICH E6 Guideline for Good Clinical Practice.Essential Functions Assemble test kits with specimen collection materials as per protocol More...

Job Description SummaryThe Sr. Research Manager is responsible for defining strategy and overseeing the execution of academic research partnerships in China. This individual provides the interface between business segment region leaders and strategic collaborative academic partners More...

Job OverviewActs as Lead Medical Writer on most types of writing projects. Prepares assigned documents in accordance with IQVIA Standard Operating Procedures (SOPs) and customer requirements as well as to the agreed timelines. Performs Senior Review of straightforward medical writing More...

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. Thi More...