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).

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.

The Scientific Specialist develops, writes, edits, and quality-controls scientific content for medical communications projects. The role requires interpreting scientific data, applying therapy-area knowledge and industry guidelines (e.g., Good Publications Practice), managing project tasks and client interactions, and mentoring/peer-reviewing work of colleagues and freelancers.

Provide project coordination support to account teams for medical communications and publications projects: track timelines and deliverables, manage publications/MedEd tracking (Datavision, iEnvision, PubStrat), organize meetings and congress submissions, maintain documentation and dashboards, monitor budgets and risks, liaise with clients and faculty, and support proposal/budget/pitch development. Bachelor’s degree preferred.

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.

Cross-check scientific information against cited references and ensure reference integrity; review/add anchor links and citation style; ensure alignment with latest local approved product label and flag off-label statements; QC essential information (ISI, brand/generic names, AE reporting), footnotes, terminology, branding, style, format, grammar, spelling and punctuation; create documentation and checklists for Asset Technical and MLR Review based on local guidelines.

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.

Responsible for authoring global CMC variation submissions, annual reports, renewals, post-approval roll-outs and responses to health authority queries. Requires proven CMC regulatory writing and submission-management experience for biological products and vaccines (M3 authoring mandatory), strong stakeholder management, and at least 5 years' industry experience.

Parexel seeks a Senior Clinical Research Associate to manage and monitor assigned oncology investigator sites throughout study setup, conduct and close-out in accordance with GCP/ICH and sponsor standards. Requires minimum 3 years monitoring experience, oncology experience preferred, strong knowledge of clinical trial operations, AE/SAE reporting, TMF documentation, and ability to travel 60–80% within the assigned US 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.

Parexel is recruiting a Scientific Specialist - Medical Information to perform literature searches (PubMed and other databases), create or update gSSRCs/FAQs, respond to escalated queries from HCPs/patients/internal teams, and liaise with stakeholders. Requires a scientific degree (PharmD/MD/PhD/Masters), strong medical writing experience (minimum 3 years producing content), knowledge of IT/digital solutions, and experience with scientific publications; therapeutic-area experience (CRM, Respiratory, Inflammation/Immunology, Oncology) is advantageous. Location listed as remote roles in Bengaluru and Hyderabad, India.

The Senior CRA will manage site activation, monitoring, and close-out activities to ensure patient safety and data quality in accordance with GCP, sponsor standards and applicable regulations. Responsibilities include AE/SAE monitoring and escalation, TMF documentation, protocol compliance, site training and enrollment support, audit/CAPA actions, investigational product oversight, and collaboration with study teams. Requires minimum 3 years site monitoring experience (preferably oncology), bachelor’s or professional life sciences degree, fluent English, valid driver’s license and passport.

Parexel is recruiting a Central Laboratory Vendor/Project Manager to support global clinical studies from the UK, Poland or Serbia. The role covers oversight of sample collection/processing/storage/shipping, vendor and CRO coordination, ICF/protocol review for sample sections, tracking and reporting of samples and data, and support through study set-up to close-out. Requires clinical research experience (6–8 years) and central laboratory and oncology experience.

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.