Designing insights-driven clinical trials. Delivering trusted solutions. Accelerating life-changing medicines. As a leading global clinical research organization (CRO), we bring our diverse perspectives together to tackle each challenge with determination, excellence, and compassion, knowing there's no limit to what we can accomplish.
When you join Parexel, you become part of a team where collaboration is real, respect is fundamental, and empathy is woven into our fabric. Through it all, at the center of everything we do, is a patient whose life could change – forever. Our unique emphasis on the patient experience drives us forward, helping treatments reach those who need them most. And together, we'll do it With Heart™.
Benefits vary by country, but Parexel is passionate about our team’s overall wellness. Our Flexible Work Program offers the choice to work from where you want and how to accommodate personal responsibilities and interests outside of work. Our Recognition Program allows colleagues and managers to acknowledge teamwork, helping each other, and helping change the lives of patients. It is our priority to put people first so we can fulfill our mission and accomplish our best work.
We believe that investing in your professional and personal development is an investment in Parexel, and we want to help you realize your full potential and career. In order to ensure the highest quality of work for our clients and our patients’ safety, Parexel takes a targeted and balanced approach to support both the immediate training needs and the long-term development investment in our employees.
Parexel is recruiting a Senior Tax Analyst. The role is listed as Hong Kong - Remote; Parexel provides services across clinical trials, regulatory, consulting, and market access.
Parexel is registering interest for a UK-based, home-based Country Study Operations Manager to manage study and country-level activities from start-up through conduct and close. Responsibilities include implementing start-up and site activation plans, recruitment strategy, study-level planning support, vendor and budget management, and communication with local teams, CROs and stakeholders. Minimum 5 years' relevant clinical trial management experience and a university degree or nursing qualification are required; senior study start-up experience is preferred.
Parexel is registering interest for Senior CRAs for UK sponsor-dedicated roles. Candidates must have at least 4 years' CRO or pharma trial experience, oncology trial experience including RECIST, and fluency in English. The role involves virtual and occasional on-site monitoring per the Study Monitoring Plan, ensuring data integrity, ICH-GCP and protocol compliance, source document verification, CRF review, IP accountability, query resolution, adverse event follow-up, and site-level coordination and documentation.
Parexel seeks a Statistical Programmer II to produce and QC derived clinical trial datasets, tables, figures, and listings using SAS (including SDTM and ADaM). The role requires adherence to SOPs and regulations (ICH-GCP, 21 CFR Part 11), participation in project start-up and documentation, and providing training/mentorship as appropriate. Competent written and oral English and a relevant degree or equivalent experience are required.
Role requires delivering high-quality statistical programming work (derived datasets, SDTM/ADaM, tables, figures, listings) and QC for low-to-medium complexity outputs using SAS; assisting project start-up and global program tracking; maintaining documentation per SOPs and regulatory standards (ICH-GCP, CDISC, 21 CFR Part 11); providing training/mentorship and participating in quality/process improvements. Location listed as Taipei (Taiwan), Shenyang (China) and remote. English competency required.
Senior Manager responsible for strategy, operations, and financial management of Parexel’s global network environment, including SD-WAN, Palo Alto firewalls, Cisco/Meraki LAN/WLAN, telecom, and AV. Role includes vendor and contract management, budgeting and cost optimization, driving standardization, security and compliance alignment, capacity and resilience planning, incident escalation, and leading engineering and operations teams. Requires 10+ years progressive experience.
The Clinical Study Administrator supports coordination and administration of interventional clinical studies within the Local Study Team, including document collection/submission to EC/IRB/regulatory authorities, eTMF and ISF setup and maintenance to ensure inspection readiness, CTMS and ANGEL updates, meeting support, and local site-level administrative tasks. Role is hybrid based in Ontario, Canada (3 days on site).
Parexel seeks an experienced Regulatory Affairs Consultant focused on CMC for vaccines/biologicals. Role supports worldwide post-approval regulatory activities (variations, renewals, market expansions, annual reports), assesses change controls, reviews QC/production study reports, coordinates submission preparation across manufacturing, supply chain, QC/QA and regulatory teams, and writes/reviews submission content. University-level life sciences background or equivalent experience, prior regulatory/CMC/technical quality experience, knowledge of vaccines/biologics, validation/QA/production experience, and fluent English required. Experience with Veeva Vault is valued.
Parexel seeks a Senior Clinical Research Associate to manage site initiation, monitoring, and closure for clinical studies (oncology experience required). Responsibilities include site management, monitoring (onsite and remote), CTMS/eTMF updates, SDV/SDR/CRF review, SAE reporting, regulatory document submission, and ensuring ICH-GCP compliance. Role requires fluency in French, proficiency in English and the ability to travel as needed.
The Director, RWD Strategy – Europe (10+ years' experience) is responsible for identifying and implementing access to real-world scientific data across selected European countries, developing client-ready RWD strategy and proposal materials, managing vendor and registry partnerships, executing regional data acquisition strategy, ensuring data governance and regulatory compliance (including EMA guidance), and supporting AI and other innovative methodologies in RWE.
Parexel is hiring for a Clinician / Clinician Manager in Shanghai and Beijing, China (remote indicated). The company works across clinical trials, regulatory, consulting, market access, and clinical development.
Responsible for managing HCP contracting activities (eg, HCP consultancy, advisory boards, steering committees) from intake through execution and close-out. Acts as delegate for HCP contracting Sponsor, coordinates with Commercial HCP contracting counterpart and internal teams (Legal, Finance, Compliance), gathers and reports planned HCP engagements to support budgeting/forecasting, and identifies process improvements. Requires 2+ years in business operations/procurement/contract administration and 2+ years healthcare industry experience; Bachelor's degree required.
Parexel FSP is seeking a Country Study Operations Manager I to lead country-level study activities (startup, conduct, close) for studies of limited complexity or portions of larger studies. Responsibilities include oversight of pCRO/CTM/SCP, site activation and recruitment planning, TMF and quality oversight, regulatory/ethics submissions support, vendor management, and implementation of local operational plans. Fluency in English and ability to travel are required. Candidates can be based in Brazil, Mexico, or Argentina.
The Investigator Payment Lead coordinates with project teams and internal stakeholders to ensure investigator/site payments are set up, authorized, processed and reported accurately for assigned studies. The role includes payment strategy input at study start-up, resolving payment discrepancies and escalations, supporting audits/inspections, analyzing payment-related data, and training team members. Position can be office-based or fully remote in Serbia, Poland or Hungary.
Parexel is hiring a Resource Planner based in Brazil (remote). The company works across clinical trials, regulatory, consulting and market access to support clinical development and therapies that benefit patients.
Acts as Parexel’s point of contact for assigned sites from identification through activation and maintenance. Key responsibilities include building relationships with investigators and site staff, conducting site qualification/remote visits, preparing and submitting IRB/IEC and MoH/RA applications, managing TMF and CTMS entries to ensure first-time quality, customizing and negotiating site-specific documents (ICFs, CDAs, CSAs), supporting site access and training, and ensuring sites are audit/inspection ready while adhering to ICH-GCP and study procedures.
The Regulatory Partner Responsible acts as the primary interface with local partners to manage third-party regulatory activities end-to-end, monitor partner performance, conduct assessments, and implement corrective actions and risk mitigation. The role supports regional regulatory teams with submission planning and keeps internal records and compliance KPIs up to date.
The Start Up Project Manager II leads start-up planning and execution for medium to large interventional clinical studies, coordinating global site activation activities, regulatory submissions, timelines and risk mitigation. Requires extensive global start-up and project management experience in clinical trials and fluency in English.
Accountable for Client FSP model management and building strong connections with function heads (Operations, Quality, Clinicians, Scientists). Responsible for conducting clinical trial innovation projects such as decentralized clinical trials (DCT) and AI/digital tool initiatives. Requires strong English communication, excellent PowerPoint skills, core team people/project management experience, and substantial clinical operations experience.
Medically qualified (MBBS/MD) role responsible for medical review of adverse event cases, MedDRA coding, supporting signal detection and validation, contributing medical content to aggregate and regulatory safety reports (e.g., PBRER/PSUR/DSUR), providing medical monitoring support, and liaising with clients and internal teams under senior physician supervision.