Parexel is hiring a Senior/Principal Statistical Programmer (Clinical SAS) in South Africa. The role requires advanced SAS and statistical programming skills, experience leading statistical programming teams, knowledge of clinical trial reporting processes and relevant regulations (ICH-GCP, 21 CFR Part 11), and strong project management, communication and mentoring abilities. Minimum experience noted: ~3.5 years for Senior level and 5+ years for Principal/Lead roles.

Parexel is hiring a Clinical Research Associate to support clinical development work, including activities related to clinical trials, regulatory, consulting, and market access.

Parexel seeks a senior regulatory affairs clinical consultant based in Japan (fully remote) to lead development regulatory strategy, manage PMDA advice/consultations, prepare and review J‑NDA/CTD dossiers (including eCTD), coordinate cross-functional teams (medical writing, translation, eCTD), and manage project timelines and client communication. Requires experience in NDA/CTD/eCTD preparation, PMDA interactions (support-level acceptable), or relevant clinical/non-clinical/CRO medical writing experience. Japanese and English business-level communication is required.

As a Senior CMC Regulatory Affairs Consultant you will support clients on CMC regulatory strategy for clinical development and marketing authorization in Japan, prepare manufacturing/CTD/MAA submission documents (new applications, variation/minor changes), draft PMDA consultation materials and respond to regulatory queries, support MF and FMA procedures, GMP compliance activities, Cartagena Act submissions, and post-approval change management. Requires 3+ years CMC regulatory experience in pharma or CRO, experience with dossier/CTD and master file preparation, biologics experience, a university degree in pharmacy or a natural science, and ability to communicate in English (TOEIC ~700 as a guideline).

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.

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.

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.

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 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.

Netguru seeks a Senior Python Developer for a long-term freelance engagement (remote — must be based in Poland). The role focuses on building Vision-Language multimodal AI features, prompt engineering, prototyping AI agents, redesigning and scaling Apache Airflow (custom operators, executors), and deploying production services with a DevOps team (Azure experience desirable). Polish language is required; good spoken/written English is expected. Rate listed up to 250 PLN/hour.

DroneDeploy is collecting interest for Account Executive-level roles based in the U.S. Candidates will own a territory/book of business, drive new logo acquisition and expansion across AEC, Energy, and emerging industries, lead full sales cycles, collaborate with sales engineering and customer success, and be expected to travel domestically 25–50% (occasional international travel). Ideal background: 1–7+ years of quota-carrying B2B SaaS sales and familiarity with tools like Salesforce and Outreach.