Clinical Research Associate II accountable for acting as Parexel's contact with assigned sites from initiation through close-out: conducting qualification/initiation/monitoring visits (on-site and remote), ensuring protocol adherence and data integrity, managing regulatory and TMF documentation, supporting site recruitment and training, participating in audits/inspections, and maintaining CTMS/EDC/IVRS/SIS records. Role requires frequent travel and site-facing activities.

Deliver medical support and medical monitoring activities for clinical studies (including medical review of data, safety/serious adverse event review, medical input to PV workflows and regulatory safety reporting). Participate in study planning, protocol and study document development, training of study teams, audits/inspections, rotas for emergency medical contact, client engagement and support business development/proposal activities. Requires medical qualification, clinical practice experience, knowledge of GCP/ICH/FDA/EMEA guidelines and a minimum of 3 years' medical monitoring or medical data review experience.

Own indirect tax filings, reconciliations, payments, and audit defense for Australia, China, India, Japan, Korea, and Singapore. Prepare returns from NetSuite extracts, post tax journal entries with SOX-ready documentation, coordinate with third-party tax vendors and Treasury, and drive process improvements to reduce compliance risk. Requires 3–5 years' indirect tax compliance experience in APAC, strong Excel and NetSuite/ERP skills, and clear English communication.

Manage early-phase clinical studies from pre-award/bid defense and start-up through implementation and close-out. Own sponsor communications, lead kick-offs, oversee site selection, IRB/EC and RA processes, monitor timelines, recruitment and data cleaning, track budgets via CTMS, prepare for audits, identify and mitigate risks, and provide oversight and training to junior project staff. Requires a science-related bachelor's (advanced degree preferred) and 2 years' PM experience with Parexel or 3–5 years in related fields; knowledge of ICH-GCP and proficiency in MS Office.

Implements and monitors clinical trials per ICH GCP and local regulations. Responsibilities include site qualification and initiation, source data verification, IP accountability, SAE verification, essential document reconciliation, audit facilitation, mentoring junior CRAs, and supporting protocol amendments and investigator site budget negotiations. Role involves on-site and remote monitoring; location indicated as Wuhan/Chengdu, China.

Responsible for end-to-end payroll processing for APJ (Australia, China, Hong Kong, Japan, New Zealand, Singapore), resolving discrepancies, maintaining payroll systems, performing reconciliations and validations, producing payroll reports, ensuring local compliance, supporting audits, and working with HR, finance and vendors. Requires 5+ years payroll administration experience in APJ and familiarity with Workday, ServiceNow and payroll data analysis.

Own and evolve CI systems that run ML workloads across GPUs and accelerators, improve reliability and reproducibility, apply automation and AI/agent-based workflows to reduce manual operations, and provide a self-service CI platform while partnering with compiler, infrastructure, and release teams. Requires 5+ years' experience and strong Python and CI/platform engineering skills.

Responsible for end-to-end site contract management across APAC, including setting contracting strategies, drafting/reviewing/negotiating CTAs and vendor contracts, site budget negotiations, contract tracking, and working closely with Clinical Operations and sponsors. Role is client-facing, requires experience in CRO/biotech/pharmaceutical settings, and involves some domestic and occasional international travel.

Parexel is recruiting a Clinical Research Associate I/II based in Chengdu (remote option). Responsibilities include on-site and remote monitoring, site initiation/qualification, regulatory document management, updating CTMS/TMF/EDC, ensuring ICH-GCP compliance, addressing site issues, and supporting recruitment and training. Candidate should have site management or equivalent clinical research experience and a degree or relevant nursing qualification.

Responsible for design and writing of trial outlines, protocols and amendments in collaboration with internal and external experts; create and deliver clinical/protocol training; establish and oversee Data Monitoring Committees and endpoint adjudication committees; maintain direct contact with investigative sites to support enrollment and address protocol questions. Requires project management/leadership experience, knowledge of GCP and regulatory requirements, and fluency in English and the host country language.

Lead strategic, multi‑stakeholder client relationships for high‑value global accounts, build tailored success plans, manage risk, and deliver measurable outcomes across retention, renewals and growth. Use Salesforce and data to provide performance visibility, support upsell/forecasting and mentor colleagues; fluent English is required. Experience with HR or payroll solutions and managing complex, multi‑country portfolios is expected.

Remote, full-time BD role requiring the candidate to be based in mainland China with legal right to work and extensive travel across Chinese mining, hardware, and energy hubs. Responsibilities include owning end-to-end sales (discovery, demos, commercial discussions, closing), maintaining pipeline and forecasts in HubSpot, feeding market intelligence to HQ, and coordinating with US BD reps. Full professional fluency in Mandarin and English is required.

Lead clinical point of contact for study execution: develop clinical documents and monitoring strategies, manage CTMS/eTMF, oversee site feasibility, start-up, enrollment, regulatory/IRB submissions, IP management, vendor oversight, CRA training and performance, and collaborate with project management, data management and QA to ensure study timelines and quality deliverables. Requires minimum 5 years clinical research experience and regional experience covering China.

The VP, Production Operations leads a global operations organization to ensure customer production programs are delivered on-time, on-quality, and on-budget. Responsibilities include defining operational readiness, executing production programs, owning supply chain strategy, driving process excellence (lean/Six Sigma), leading digital/ERP initiatives and AI use-cases, and building scalable teams. Remote role with frequent travel (~25–40%) to supply regions including India, China, Mexico, Japan, and the US.

Canonical's Kernel Team seeks a Test Engineer to own kernel testing strategy and infrastructure across many concurrently supported Ubuntu kernel versions. Responsibilities include designing and maintaining test plans and long-lived test suites, building automated test frameworks (stress tests, fuzzing, code coverage, regression detection), developing CI/CD pipelines, and collaborating with kernel engineers. Required skills include significant Python experience, familiarity with Linux kernel internals and system-level testing frameworks, CI/CD systems, git, and strong English communication. Role is remote within APAC with office options in Beijing (China) and Taipei (Taiwan); occasional travel (twice a year) is required.

Parexel is recruiting a CRA II (FSP) for cell therapy to perform site monitoring and onsite activities, ensure data quality (SDV, query resolution), manage drug and study supplies, report SAEs, support site selection and investigator training, and prepare for audits/inspections. Requires a bachelor's in biological/health sciences (or equivalent), minimum 2 years' CRA experience, knowledge of ICH-GCP/GCP and proficiency in English and the host country language.

Parexel CRA II to perform site monitoring and onsite activities per monitoring plan, manage study and drug supplies, perform SDV, ensure data/query resolution, report SAEs, contribute to site selection and train site staff. Requires minimum 2 years CRA experience, bachelor's in biological/healthcare field, fluent English and host-country language, and knowledge of GCP/ICH and clinical drug development.

Accountable for full site lifecycle activities (site identification through close-out) including qualification, initiation, on-site and remote monitoring, TMF and regulatory document management, CRF and SAE follow-up, site training, and ensuring compliance with ICH-GCP and study procedures. Requires experience in site management/clinical research, use of CTMS/EDC/EDMS, strong communication and problem-solving skills, and ability to travel extensively.

Responsible for managing clinical operations aspects of studies including study start-up, site selection, monitoring oversight, TMF quality, vendor coordination, recruitment/retention monitoring, risk management, audits/inspections and cross-functional liaison. Ensures compliance with ICH-GCP, SOPs and study procedures and provides leadership to virtual project teams.

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.