Parexel is hiring Project Leader (PM) and Senior Project Leader (SPM) roles to provide leadership for mid-to-large global clinical trial projects across therapeutic areas. Responsibilities include leading project teams, managing day-to-day operations, project scheduling, resource and budget management, coordinating team activities, and supporting the full clinical development process through regulatory submissions. Minimum requirement is 2+ years leading global clinical trials in project management (CRO preferred); advanced degree preferred. Roles are homebased in the United States.

Responsible for managing clinical operations aspects of studies including study start-up, site selection, monitoring oversight, TMF quality, vendor coordination, recruitment/retention monitoring, risk management, audits/inspections and cross-functional liaison. Ensures compliance with ICH-GCP, SOPs and study procedures and provides leadership to virtual project teams.

Parexel is recruiting a Global Clinical Trial Lead accountable for setup, conduct and delivery of assigned phase 3 oncology or inflammation trials. Responsibilities include trial planning and feasibility, leadership of the trial team, oversight of GCP and regulatory compliance, recruitment and risk mitigation planning, vendor oversight, budget and safety reporting, TMF archiving, and coordination with medical writing and other functions. Role is fully remote and requires at least 5 years' relevant clinical trial management experience.

The Site Payment Lead coordinates site payment activities across studies and project teams, manages payment setup and modifications within investigator payment systems, analyzes agreements and budgets, resolves payment discrepancies, prepares reports, supports audits/inspections, and identifies process improvements. Requires a bachelor’s degree, strong English (advanced/excellent), proficiency in MS Office (especially Excel), and typically 4+ years of relevant CRO/finance/project experience.

Parexel is recruiting an experienced Clinical Project Leader / Senior Project Leader to manage global biotech clinical trials from planning through delivery. The role requires CRO clinical trial project leadership experience (Phase I–III), strong financial and client-management skills, therapeutic area expertise (oncology required; dermatology, women's health, neurology, rare disease or radiopharmaceuticals desirable) and proficiency with ICH/GCP and standard eClinical systems. Remote opportunities are available in specified EMEA countries.

The Local Study Associate Director (LSAD) is responsible for leading and optimizing Local Study Teams at the country level to deliver clinical trial commitments (site identification, qualification, initiation, monitoring, closure and documentation) in compliance with ICH-GCP and local regulations. Role includes oversight of CTMS/eTMF, regulatory submissions, budgeting and vendor/stakeholder management. Minimum 3 years' relevant experience (Development Operations/CRA), bachelor's degree preferred; ability to travel nationally and internationally as required.

Responsible for country-level study activities (startup, conduct, close) on low-to-moderate complexity studies or portions of larger studies. Key duties include leading local study teams, overseeing pCRO/CTM/SCP, managing country plans (timelines, budget, risk, quality), supporting regulatory/EC submissions, ensuring TMF/ISF completeness, driving site recruitment and data cleaning activities, and ensuring ICH-GCP and SOP compliance. Role requires travel as needed and fluency in English. Education/experience: Bachelor's + 5 years or Master's + 3 years (per vacancy).

Parexel is recruiting a Country Study Operations Manager I to lead country-level study activities (start-up through close) for trials with limited complexity or portions of larger studies. The role includes oversight of pCROs/CTMs/SCPs, site activation and recruitment planning, TMF/ISF oversight, regulatory and ethics submissions support, vendor management, quality and audit readiness, and implementation of decentralised trial tools (eConsent, eISF, remote SDV/SDR). Candidates must be based in Brazil, Mexico or Argentina, have experience with US/Canada, be fluent in English, and have the minimum relevant clinical trial operational experience stated in the posting.

FSP Senior Regulatory Affairs Associate supporting global and local regulatory teams for products in Australia (and experience including New Zealand). Responsibilities include post‑authorization lifecycle activities (variations, renewals, PSURs), preparing local submission documentation (Module 1), managing health authority interactions, impact assessments for CMC/label changes, use of document management systems, project and client reporting, and supporting regulatory compliance and inspections. Requires a bachelor’s in a scientific/technical discipline and 3+ years’ industry experience in Australia/NZ; role is remote with periodic office attendance.

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.

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 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 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.