Lead Clinical Trial Operations Manager Jobs in Beijing

Iterative Health is a healthcare technology and services company powering the acceleration of clinical research to transform patient outcomes. The Iterative Health Site Network is a premier network of 70 clinical research sites across US and Europe accelerating the path to market for gastrointestina...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionJoin Us as a Senior Regulatory Affairs Specialist 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...

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Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionJoin Us as a Manager Regulatory Affairs - Make an Impact at the Forefront of InnovationThe Manager Regulatory Affairs manages a team within the department and provides innovative solutions including regulatory expertise and...

Job DescriptionThis role is primarily accountable for the end-to-end performance and project management for assigned protocols in a country in compliance with ICH/GCP and country regulations company policies and procedures quality standards and adverse event reporting requirements internally and ext...

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 healthier cleaner and...

Prepare high-quality and accurate China-specific regulatory and clinical documents in accordance with regulatory requirements based on policies of global R&D and China Development.Serve as local coordinator to streamline the communication between China project team and global medical writing team (S...

Job Description SummaryProvides regulatory strategy and direction to the business regarding healthcare industry regulatory requirements for product launch premarket submissions/registrations and postmarket compliance working closely with healthcare regulatory bodies globally. Interprets simple inter...

Department: MRQLocation: BeijingThe position Perform medical writing tasks for regulatory documents (e.g. HA consultation package bridging report clinical summaries) including Chinese version proofreading. Take overall responsibility to drive local clinical trial disclosure on specific trial/proj...

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...

Job DescriptionROLE RESPONSIBILITIESPortfolio strategy building & evaluation: Developing portfolio strategy for responsible therapeutic field under the guidance of Vx head. Cooperating with cross-functions especially BD/BU to evaluate their mature products and determine which one is needed to transf...

Senior Medical Director Oncology The IQVIA Oncology Center of Excellence a hub of Oncology clinical innovation is looking for exceptional Board-Certified oncologist to join our team as a Medical Strategy Lead to help us expand our Oncology portfolio and advance this dynamic and rapidly expanding are...

MAIN REPONSIBILITIES / DUTIESMaximize the value of Pfizer products to Chinese patients and health care professional within Pfizers vision and mission. Develop KOL engagement strategy and action plan. Establish regional platform and channel with China regional academic organization in defined therape...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionAt Thermo Fisher Scientific you will 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 a...

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...

Career CategoryRegulatoryJob DescriptionRegulatory Affairs Manager- ChinaReporting to: Head of Regulatory Strategy China RABased in: BeijingJob DescriptionApplying obtaining and maintaining regulatory approvals for products within Amgens portfolio including CTN MAA renewal variations of products lif...