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).

Senior Clinical Project Manager (FSP) role at Parexel. Location listed as Shanghai, China with remote indicated. Parexel provides clinical trial, regulatory, consulting, and market access services.

Parexel seeks a Program Coordinator to support clinical research and medical communications activities including managing program timelines, publications and medical education tracking, organizing meetings and congress submissions, maintaining documentation and dashboards, and monitoring budgets and risks. Requires a bachelor's degree (or equivalent) and 3+ years of project/team coordination experience; experience with Datavision, iEnvision or PubStrat is listed.

Parexel is hiring a Biostatistician II to coordinate and lead statistical activities for clinical trials, including analysis plans, randomizations, statistical reports, QC of datasets/tables/listings, and support for DMC reviews. Role requires SAS programming experience and advanced statistical knowledge; PhD or MS in statistics (with corresponding experience) is specified. The position includes client interaction, occasional travel to meetings, and contribution to business development and study design.

Parexel is hiring a Study Manager (FSP). The company provides clinical development solutions including clinical trials, regulatory, consulting, and market access. Role locations listed as Beijing and Shanghai with remote work.

Parexel seeks a Clinical Project Manager (FSP) for work based in China (Beijing/Shanghai, remote). The role relates to clinical trials and clinical development and references regulatory, consulting, and market access activities. Employer: Parexel.

Parexel seeks a Senior Associate with a Master's/PhD and at least 3 years' experience in pharma, consultancy, HTA/access, or academia. The role involves designing evidence-generation plans, conducting statistical analyses (e.g., GLMs, survival analysis, NMA, Bayesian methods), developing technical documentation and economic models, and contributing to cross-functional Access/HTA strategies. Proficiency in R and GitLab is required; familiarity with SAS, Python, WinBUGS, or JAGS is a plus.

The Senior Clinical Research Associate will manage and monitor assigned investigator sites from activation through close-out, ensure compliance with protocol/GCP/FDA/local regulations, support enrollment, handle SAE reporting and TMF documentation, perform onsite and remote monitoring, and drive corrective actions and audit responses. Minimum 3 years monitoring experience required; travel 60–80% within area.

The Site Monitor II performs on-site and predominantly virtual monitoring per the Study Monitoring Plan, ensures protocol and regulatory compliance, manages site documentation in CTMS/EDC/TMF, follows up on CRF queries/SAEs, supports site training and readiness for inspections. Requires minimum 3 years' clinical monitoring experience and English proficiency.

Implements and monitors clinical trials (on-site and remotely), assesses and initiates investigative sites, performs SDV and source file reconciliation, reviews IP accountability and SAE reporting, updates trial tracking systems, facilitates audits, and mentors junior CRAs. Duties include communicating with sites, escalating and resolving site/trial issues, and supporting protocol amendments and site budget negotiations as needed.