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 oncology investigator sites from activation through close‑out to ensure patient safety and study quality in accordance with GCP, ICH, and sponsor standards. Role requires at least 3 years' clinical site monitoring experience (preferably 2 years in oncology), proficiency in English, extensive travel (60–80%), and responsibilities including AE/SAE handling, TMF documentation, site training, CAPA remediation, and audit support.

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.

Parexel FSP is hiring CRA II or Senior CRA to manage site activation through close-out for sponsor clinical trials. Responsibilities include site monitoring, ensuring compliance with ICH/GCP and applicable regulations, AE/SAE monitoring and liaison with Drug Safety, audit support and CAPA follow-up. Requires a bachelor's/professional degree in life sciences (or nursing/pharmacy/medical background), extensive knowledge of clinical trial methodologies and a minimum of 3.5 years' relevant site monitoring experience (advertised). Oncology experience preferred.