Job Description Support of the company Portfolio (85%) Lead cross-functional project teams in the strategy planning, execution, and delivery of China new product development projects. Develop project milestones and deliverables; prepare reports that summarize key progress
Job Description SummaryThe Senior Director of Risk Management within Global Pharmacovigilance provides strategic leadership and expert oversight for global product safety risk management, benefit–risk evaluation, and safety signal governance across the product lifecycle. This role ensures the highest
Join our Team About us: Ericsson is at the forefront of wireless communication technology, driving innovation in baseband design and Radio Access Network (RAN) testing. We are seeking a motivated and adaptable intern to join our
Reports to: Quality Manager Department: Elektron Contributions Team Applications are invited for the position of Principal Quality Engineer. This position is to be based in Beijing China and is offered on local terms and conditions. Relocation
At Johnson & Johnson,we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal.Through our
Job Description Clinical and Regulatory Strategy Development o Drive the clinical development, expand portfolio, and speed up registration o Get alignments with Global PDT and obtain CDRC/LDRC endorsement. o Execution clinical & registration strategy Regulatory related
Overview As a Sr Planner/Planning Lead at Linesight, you will work with highly experienced, culturally diverse, and passionate teams nurturing a strong social dynamic and a shared sense of achievement. You will gain vast industry experience
Keen to become part of a truly global, collaborative team of professionals? Your journey begins here. We are currently recruiting interns to join Hogan Lovells Cadwalader for the Beijing office in Corporate & Finance practice. SCOPE
Keen to become part of a truly global, collaborative team of professionals? Your journey begins here. We are currently recruiting interns to join Hogan Lovells Cadwalader for the Beijing office in Intellectual Property practice. SCOPE OF
ABOUT US Xsolla is a global commerce company with robust tools and services to help developers solve the inherent challenges of the video game industry. From indie to AAA, companies partner with Xsolla to help them
Overview Class: Full-time AND Permanent Legal Entity: StoneX Financial Inc. (FCM Division) Company Overview: Connecting clients to markets – and talent to opportunity. With 5,400+ employees and over 80,000 institutional, commercial, and payments clients, we operate
Minimum qualifications: Bachelors degree or equivalent practical experience. 8 years corporate secretarial, corporate legal or paralegal/legal specialist experience at a law firm, service provider or in-house legal department of a multi-national company. Ability to communicate 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
Job Description SummarySystems engineering is a cross-functional engineering discipline centered on an approach, mindset, and process. All activities that consider both the business and the technical needs of the customers with the goal of providing a
Job title职位名称: M&S Graduate Program-Quality Trainee Location工作地点： Beijing 北京 About Sanofi We’re an R&D-driven, AI-powered biopharma company committed to improving people’s lives and delivering compelling growth. Our deep understanding of the immune system – and innovative
Work Your Magic with us! Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich
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
Summary of Responsibilities: Site management responsibility for clinical studies according to Fortrea’s Standard Operating Procedures, ICH GCP Guidelines, applicable project plans and Sponsor requirements, including verification of study training records. Conducts site monitoring responsibilities for clinical trials
Job Overview: The Senior Clinical Research Associate II (Sr CRA II) is responsible and accountable for site monitoring and site management for clinical studies according to Fortrea, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. The Sr
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,