Document Management Jobs in Beijing

We are seeking a detail-oriented and organized Document Control professional to join our team in Dammam Saudi this role you will be responsible for managing and controlling all project documentation ensuring compliance with established procedures and standards.Manage organize and control project do...

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...

The Opportunity:Workers engaged for short-term needs or specific projectsMain responsibilities职责描述As a QualiPSO CMS Business Owner 作为QualiPSO 系统CMS 流程专家undefinedOversee the local implementation and management of the QualiPSO Clinical Management System (CMS).undefinedEnsure the CMS meets...

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...

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...

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...

At Johnson & Johnsonwe believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented treated and curedwhere treatments are smarter and less invasive andsolutions are our expertise in Innovative Medicine and MedTech we are unique...

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...

What youll do (responsibilities)Lead legal strategy for generative AI products including driving design reviews advising on risk mitigation and embedding legal input into product planning and delivery cycles.Own and manage China-specific AI-related regulatory filings such as algorithm disclosures LL...