1,039 full time remote jobs in China available for work from home. Apply for positions such as R&D - Senior Technical Leader, R&D - Senior Manager, R&D - Senior Technical Leader and more! Discover the best work-from-home or hybrid jobs.
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Design and develop embedded firmware and software features for IoT applications, including sensor integration and data pipeline management. Conduct system-level testing and security validation while utilizing AI-assisted tools to accelerate development and debugging processes.
Lead a team of development and test engineers to drive the execution and delivery of IoT solutions while ensuring high standards of quality and security. Establish Agile processes and foster a culture of collaboration, innovation, and responsible AI-assisted development.
The Senior Technical Leader will design and implement test scripts, fixtures, and validation strategies for IoT hardware and software platforms. They will perform security penetration testing and collaborate with cross-functional teams to ensure product quality and performance.
You will conduct clinical trial monitoring activities, including site visits and ensuring protocol compliance and data integrity. Additionally, you will collaborate with investigators and site staff to facilitate study conduct and prepare essential study documentation.
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The CRA I is responsible for coordinating clinical trial monitoring activities, maintaining study documentation, and ensuring compliance with protocols and regulatory requirements. They will also manage sponsor queries, monitor study cost efficiency, and build collaborative relationships with clinical investigators and site staff.
The CRA I is responsible for coordinating clinical trial monitoring activities, maintaining study documentation, and ensuring compliance with protocols and regulatory requirements. They will also manage sponsor queries, monitor study cost efficiency, and build collaborative relationships with clinical investigators and site staff.
The representative is responsible for executing academic promotion plans, conducting professional customer visits, and facilitating clinical communication for pharmaceutical products. They must also collect market insights, manage resources, and ensure all activities comply with national regulations and company policies.
The Programmer Analyst II will serve as a lead programmer on clinical trial projects, overseeing statistical and bioinformatics programming from design through analysis. They are responsible for implementing study strategies, ensuring process efficiencies, and providing guidance to junior team members.
You will conduct clinical trial monitoring activities, including site qualification, initiation, and close-out visits. Additionally, you will ensure protocol compliance, maintain data integrity, and collaborate with investigators to facilitate smooth study conduct.
The Account Expert will act as a trusted advisor to top-tier customers, developing digital marketing strategies to increase revenue and drive success. They will also manage client onboarding, conduct quarterly business reviews, and provide ongoing strategic guidance to ensure business goals are met.
The HR Services Administrator serves as a primary point of contact for employee inquiries and manages HR operational processes throughout the employee lifecycle. This role ensures accurate service delivery, maintains data integrity in HR systems, and collaborates with stakeholders to improve HR processes.
The HR Services Administrator serves as a primary point of contact for employee inquiries and manages HR operational processes throughout the employee lifecycle. This role ensures accurate service delivery, maintains data integrity in HR systems, and supports benefits and pension administration.
The CRA II is responsible for conducting clinical trial monitoring activities, including site qualification, initiation, and close-out visits. They ensure protocol compliance, data integrity, and patient safety while collaborating with investigators and site staff.
The Team Lead of Account Experts will lead and coach a team while overseeing the Chinese-speaking book of business to ensure customer health and retention. They are responsible for driving CS strategy, managing escalations, and ensuring APAC customers successfully achieve their goals with the platform.
The Programme Associate will act as a thought partner to the Programme Manager to help shape and deliver regional strategies. They will build trusted relationships with communities, grantee partners, and stakeholders while translating field observations into strategic insights.
The Operations Coordination Manager will lead regional operations across Australia, Korea, Japan, and China, ensuring the seamless movement of pharmaceutical shipments. They will manage Service Centers, oversee partner performance, and act as a key decision-maker for daily operational and logistics challenges.
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The Territory Sales Manager is responsible for driving sales growth in North China and managing key opinion leaders to ensure market success. They will also collaborate with distributors to manage channel inventories and execute regional sales strategies.
The Marketing Specialist will manage localized content and social media campaigns for the Greater China market across platforms like WeChat and Xiaohongshu. They will also oversee KOL collaborations, livestreaming events, and paid media execution to drive growth.
The role involves managing localized content for digital channels like WeChat and Xiaohongshu while overseeing KOL collaborations and community engagement. Additionally, the specialist will coordinate livestreams, events, and paid media campaigns to support growth initiatives in the Greater China market.
The Inside Sales Representative will proactively engage target patients through digital channels to provide product information, manage sales opportunities, and drive conversions. They are responsible for maintaining accurate customer data in CRM systems and collaborating with marketing teams to enhance patient outreach and service quality.
The role involves proactive patient outreach via phone and digital channels to manage the full sales cycle, from lead identification to final conversion. Additionally, the representative will manage customer data in CRM systems and collaborate with marketing teams to optimize digital patient engagement strategies.
The manager will design and iterate on financial derivative products, including perpetual contract mechanisms, margin systems, and liquidation protocols. They are also responsible for establishing risk parameter frameworks, monitoring platform exposure, and managing the full lifecycle of new asset listings.
You will be responsible for finding new audio data sources and managing the cloud infrastructure for the ingestion pipeline. You will also collaborate with scientists to optimize data quality and scale while defining the dataset roadmap for AI products.
The Technical Specialist will develop complex suppliers and products to meet customer requirements by building strong relationships with internal and external stakeholders. They will lead quality improvement plans, conduct supplier audits, and provide manufacturing consultation to ensure zero-defect components.
The Clinical Research Associate implements and monitors clinical trials to ensure compliance with regulatory requirements and ICH GCP guidelines. They are responsible for site qualification, data verification, and facilitating the resolution of clinical trial issues.
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The role involves achieving sales targets for assigned hospital clients, managing key accounts, and identifying new business opportunities. It also requires collecting market intelligence, coordinating internal resources for customer support, and developing long-term business plans for the assigned territory.
The representative is responsible for executing academic promotion plans, conducting professional customer visits, and facilitating the rational use of pharmaceutical products. They must also collect market insights, manage promotional activities, and maintain compliance with national regulations and company policies.
The role focuses on developing complex suppliers and products to meet customer requirements through strong partnerships with supply chain, engineering, and manufacturing teams. Responsibilities include leading quality improvement plans, conducting supplier audits, and providing manufacturing consultation to ensure zero-defect components.
You will oversee and manage clinical trial monitoring activities to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice standards. Additionally, you will conduct site visits, provide training to site staff, and collaborate with cross-functional teams to ensure accurate data collection.
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