Parexel seeks a Statistical Programmer II to produce and QC derived clinical trial datasets, tables, figures, and listings using SAS (including SDTM and ADaM). The role requires adherence to SOPs and regulations (ICH-GCP, 21 CFR Part 11), participation in project start-up and documentation, and providing training/mentorship as appropriate. Competent written and oral English and a relevant degree or equivalent experience are required.

Parexel is hiring for a Clinician / Clinician Manager in Shanghai and Beijing, China (remote indicated). The company works across clinical trials, regulatory, consulting, market access, and clinical development.

Lead onsite factory quality activities for suppliers in East China, including NPI and mass production oversight, supplier audits, root cause analysis, performance metrics, and driving continuous improvement. Requires a bachelor's degree in a related field and a minimum of 5 years' quality experience.

Manage the full employee lifecycle and act as primary HR contact for global clients and workers. Provide HR and benefits guidance, prepare employment documentation, ensure compliance with local labor law and GDPR, coordinate with payroll/benefits vendors, support work permit processes, lead HR initiatives and projects, and generate reports and audit support. Prefer candidate based in Shanghai with ~5-6 years' relevant HR experience and domestic Chinese HR qualifications as an advantage.

Responsible for execution of site start-up strategy across APAC countries (Australia, Singapore, South Korea, Taiwan, China). Accountable for IRB/EC and CA/MoH submissions, ICF customization, IMP release packages, milestone tracking, translations coordination, training/mentoring, and cross-functional stakeholder communication. Requires a bachelor's in life sciences or RN and at least 5 years' start-up experience.

The Site Start Up Lead (APAC) is responsible for execution of site start-up strategy and planning across APAC (Australia, Singapore, South Korea, Taiwan, China), including IRB/EC and CA/MoH submissions, ICF customization, IMP release packages, milestone planning/tracking, contract and budget negotiation, stakeholder communication, and mentoring/training of less-experienced staff. Minimum 5 years' start-up experience is required.

Lead role accountable for site start-up strategy and execution including IRB/EC and CA/MoH submissions, ICF customization, IMP release packages, milestone planning, risk mitigation, stakeholder coordination, contract and budget negotiation, document translations, and training/mentoring. Requires a bachelor's in life sciences (or RN) and a minimum of 5 years' start-up experience.

Role based in APAC (Australia/Singapore/South Korea/Taiwan/China). Accountable for end-to-end site start-up delivery: activation readiness strategy, IRB/EC & CA/MoH submissions, ICF customization, IMP release packages, contract/budget negotiation, translations, milestone tracking, risk mitigation, stakeholder engagement, training and mentoring. Requires a bachelor's (or RN/equivalent), 5+ years start-up experience (including SU Lead or PM experience) and 2+ years in project milestone/resource management. Fluency in English required.

Accountable for execution of APAC site start-up strategy and planning, coordinating document collection and approvals, IRB/EC and regulatory submissions, ICF customization, IMP release packages, translations, and milestone tracking. Acts as SME and trainer for site start-up processes and partners with cross-functional stakeholders to manage risks and timelines. Role can be based in Australia, Singapore, South Korea, Taiwan, or China (remote options noted).

Lead Data Management contact for assigned clinical studies: develop CRF specifications, oversee database build and UAT, define edit checks, perform/query data review and medical coding (MedDRA/WHODrug), manage TMF documentation, run study metrics and reporting, coordinate with sponsors/vendors, and provide training. Requires 8+ years' experience and professional English; experience with Medidata Rave and Veeva.

Implements and monitors clinical trials at investigative sites (on-site or remotely), assesses site qualification, verifies clinical data and SAE reporting, and ensures IP accountability. Maintains trial documentation and tracking systems, facilitates audits, mentors junior CRAs, and supports related clinical operations tasks such as protocol amendments and site budget negotiation.

Role to provide technical support for Mapbox's automotive partners in China, troubleshooting map and navigation issues, debugging Android (Kotlin/Java) code, monitoring GitHub issues, collaborating with engineering and documentation teams, and converting user feedback into product actions. Requires native-level Mandarin and English and experience with automotive OEMs or Tier 1 suppliers.

Enterprise Solutions Architect partnering with sales and customers to perform technical discovery, design scalable architectures using Mapbox SDKs/APIs, respond to RFI/RFQ, deliver PoC/PoV, and support adoption. Requires native-level Mandarin and English, 5+ years in solutions architecture or customer-facing engineering/consulting, and willingness to travel up to 25%.

Build and operate Luxor's next-generation backend services in Golang, focusing on high-concurrency, long-lived network services, real-time workload distribution, and scalable, fault-tolerant system architecture. Requires 3+ years of backend engineering with Go, experience with Docker/Kubernetes, Linux troubleshooting, performance optimization, and proficiency in English for asynchronous collaboration.

Join Veeva's China Business Consulting Group to lead workstreams on commercial strategy and transformation projects for life sciences customers. Responsibilities include end-to-end delivery, client-facing engagement, mentoring associates, and contributing to proposals; requires 3+ years' consulting or in-house operations experience and strong commercial, analytical, and project management skills. Ability to travel (~50%) and right to work in China required.

Canonical seeks an IoT Field Engineer based in Shenzhen to support customers in China and the broader Asia-Pacific region. The role requires experience with Ubuntu and Linux (including kernel, BSPs, bootloaders, packaging), embedded and IoT deployments, knowledge of x86/ARM SoCs, IoT security, cloud services, and technical presales work such as presentations and RFx responses. Travel up to ~30%.

Parexel is hiring a Clinical Research Associate to support clinical development work, including activities related to clinical trials, regulatory, consulting, and market access.

Parexel is recruiting for its 2026 China campus talent pool (CDA/SP/PSA). The opportunity relates to clinical development functions including clinical trials, regulatory, consulting and market access. Positions are listed for China with Beijing/remote location mentioned. Parexel emphasizes improving global health and contributing to therapy development.

Parexel is hiring a Payment Specialist. The role is based in Beijing, China (remote). Parexel provides clinical development services including clinical trials, regulatory, consulting, and market access.

Parexel is hiring a Clinical Research Associate II (FSP) to support clinical development solutions including clinical trials, regulatory, consulting, and market access. The role is listed as China — Guangzhou (remote).