As a Regulatory Affairs Consultant (Regulatory Intelligence), you will monitor, analyze, and translate local, regional, and global regulatory changes into actionable insights for global and local regulatory teams. The role involves impact assessments, preparing briefings/newsletters, external engagement with regulators and industry forums, and collaboration with functions such as Quality, Pharmacovigilance, and Medical Affairs. The position can be fully home based or office based and requires fluency in English.

Parexel seeks Clinical Research Associates to monitor clinical trial sites via on-site and remote visits, build relationships with investigators, manage site-level study documentation and visit reports, collaborate with cross-functional teams, implement corrective actions, and ensure sites remain audit- and inspection-ready. Role is home-based with eligibility limited to candidates residing in São Paulo, Rio de Janeiro, Curitiba, or Porto Alegre. Requires a bachelor’s degree in life sciences/pharmacy/nursing or related field, fluent English and Portuguese, minimum 1 year CRA experience, ability to travel, and a valid driver’s license.

Implements and monitors clinical trials at investigative sites (on-site or remotely), assesses site qualification, verifies clinical data and SAE reporting, and ensures IP accountability. Maintains trial documentation and tracking systems, facilitates audits, mentors junior CRAs, and supports related clinical operations tasks such as protocol amendments and site budget negotiation.

Parexel is hiring a Clinical Research Associate II (fully decentralised in the UK). The role conducts qualification, initiation, monitoring and termination visits; manages site relationships and recruitment strategies; reviews data quality, drug accountability and regulatory documentation; and ensures compliance with protocol, SOPs, GCP and applicable regulations. Requires site management/clinical research experience, ability to perform monitoring independently, a relevant degree and strong communication and computer (CTMS/EDMS/MS Office) skills.

Principal Consultant in HEOR/Health Economics & Modelling with responsibility for advanced modelling leadership, acting as Project Director on complex multi-jurisdictional projects, supporting HTA submissions (e.g., NICE, SMC, CADTH, G-BA), driving business development, and developing team members. Requires 10+ years' experience, expertise in Excel/VBA and R, knowledge of HTA guidelines, and fluency in English.

Parexel Study Operations Manager II / Senior Clinical Operations Leader (Canada, remote across Quebec, British Columbia, Ontario) responsible for study- and country-level operational delivery from startup through conduct and close. Duties include leading local study teams, overseeing CROs and country trial managers/site care partners, managing startup and recruitment plans, vendor oversight, handling site activations/escalations, quality and metrics review, and regulatory/ethics submission coordination. Education/experience requirement: Bachelor's degree with minimum 5 years relevant operational clinical trial experience, or Master's (MSc/MBA) with minimum 3 years.

Responsible for leading country-level study activities (startup, conduct, close) for assigned studies in Canada, supporting Global Study Managers, overseeing pCRO/CTM/SCP and vendors, managing country plans (timelines, budget, risk, quality), ensuring TMF completeness and regulatory compliance. Requires fluency in English, travel as required, and relevant clinical trial study management experience.

Responsible for managing country deliverables and timelines for assigned protocols in compliance with ICH/GCP and local regulations; oversight of budgets, negotiation and completion of Clinical Trial Research Agreements (CTRA), payment tracking and reconciliation; execution of country regulatory submissions and interactions with IRB/IEC/Regulatory Authorities; coordination with CRMs/CRAs/CTCs, vendors and HQ; and mentoring/training of local teams. Minimal travel required.

Accountable for project management and performance of assigned clinical study protocols in country, acting as point of contact between Country Operations and the clinical trial team. Requires 5+ years clinical research experience (CRA experience preferred), responsibility for CTMS/eTMF compliance, local risk management, vendor and investigator collaboration, and up to 30% travel. Bachelor’s degree required; advanced degree preferred.

Senior Clinical Research Associate (remote, all Canada locations) responsible for site management, monitoring, and close-out of assigned investigator sites to ensure patient safety and quality study execution per GCP, ICH and sponsor standards. Requires minimum 3 years of site monitoring experience (Oncology preferred), fluency in English and local language(s), and ability to travel 60–80%.

Parexel seeks a Clinical Research Associate or Senior CRA to manage site initiation, monitoring (onsite and remote), and closure for oncology studies in the US. Responsibilities include ensuring ICH-GCP compliance, site management, CTMS/eTMF updates, SDV/SDR/CRF review, SAE reporting, drug accountability, and participation in local study teams. Cell therapy experience is strongly preferred.

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.