Parexel seeks a Senior Clinical Research Associate for UK-based sponsor-dedicated roles. The position requires a minimum of 4 years' CRO/pharma trial experience, oncology trial experience including RECIST, and fluency in English. Responsibilities include monitoring per the Study Monitoring Plan (majority virtual with supplementary on-site visits), source document verification, CRF/data review, IP accountability, regulatory and ICH-GCP compliance, query resolution, and collaboration with Site Managers to ensure sites are inspection-ready.

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.

The iCRA will act as Parexel’s primary contact for assigned sites during start-up and maintenance phases, leading site identification through activation, preparing and submitting IRB/IEC and MoH/RA applications, ensuring TMF/CTMS document quality and compliance with ICH-GCP, customizing ICFs/translations, supporting site training and system access, and managing site issues and timelines.

Senior Health Economics Modelling Consultant role in the UK requiring 8+ years' experience in health economics (cost-effectiveness and budget impact modelling), proven project leadership and client management. Technical skills expected include Excel/VBA, R and/or SAS, familiarity with HTA guidelines, generative AI tools for modelling, and strong scientific writing and business development capabilities.

The role leads local/regional trial activities including trial preparation, conduct and closeout, ensuring compliance with GCP/ICH and local regulations, budget and vendor oversight, site selection and patient recruitment planning, TMF archiving and submission of clinical trial reports. Requires a university degree in biomedical/life sciences and several years of relevant clinical trial project management 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.

Parexel seeks a Training Development Lead/Manager for a 12-month fixed-term contract (UK, remote) to design, develop, deploy and maintain global training for clinical research, pharmacovigilance and regulatory functions. Requires minimum 5 years designing and delivering learning solutions, clinical trials/pharmaceutical experience, instructional design skills, and proficiency with Articulate and related e-learning tools.

Parexel FSP seeks Investigator Contracts Lead I for Brazil, Mexico, and Argentina (remote). Responsibilities include negotiating clinical trial agreements and site budgets, managing Per-Subject Cost (PSC) processes, leading study-level site contracting activities, partnering with Legal/Finance/pCROs, and overseeing other contracting professionals. Requires Bachelor's degree or equivalent, 5+ years in clinical development operations or clinical trial outsourcing, experience with clinical study budgets and CTA negotiation, and fluency in written and spoken English.

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.

Parexel is seeking an Investigator/Site Contracts Lead responsible for negotiating and executing site contracts and budgets, managing the Per-Subject Cost process, overseeing other contracting staff on assigned studies, and partnering with Legal, Finance, CROs and study teams. Requires experience in clinical study budgets and contract negotiation, compliance with ICH-GCP, strong communication and stakeholder management; Bachelor’s + 5+ years (or JD + 2+ years) in clinical development operations or outsourcing.

Responsible for developing, negotiating, tracking and executing global clinical study agreements with investigational sites and investigators, leading study-level site contracting activities, overseeing site budget processes, and partnering with Legal, Finance and CROs to manage escalations and improvements. Requires experience in clinical study budgets and contract negotiation, fluency in English, and a minimum of 2 years' relevant experience (2+ years with Juris Doctorate or 5+ years with Bachelor's degree).

Work on health economic models and country adaptations to evaluate cost-effectiveness of health technologies for reimbursement. Tasks include model building and checking using software tools, systematic literature/HTA searches, data analysis, and supporting senior team members. Requires a relevant master's degree, strong Excel/VBA skills, programming experience (SAS, R advantageous), and fluent English. Approximately 2+ years' relevant experience is indicated as an advantage.

Lead and manage multiple HEOR projects and a service line, ensure project profitability and client satisfaction, mentor staff, drive business development and thought leadership, and support implementation and identification of AI-driven HEOR methodologies. Requires substantial life sciences/consulting experience (15+ years overall, 10+ years management) and fluent written/verbal English.

Parexel seeks a Regulatory Affairs Consultant to develop and execute regulatory strategies, lead health authority interactions and manage regulatory submissions (INDs, annual reports, safety submissions) for a dedicated pharma client. Requires minimum 5+ years in regulatory affairs, strong knowledge of FDA and ICH guidelines, experience with electronic submission systems (e-STARs), and ability to work independently within cross-functional teams.

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 seeks a Senior Regulatory Project Manager to partner with Global Regulatory Leads to develop and execute forward-looking, globally aligned regulatory strategies and plans across development and post-marketing. The role includes facilitating Global Regulatory Subteam (GRST) meetings, translating strategy into actionable milestones, managing complex timelines and risks, and supporting regulatory submissions (IND/BLA/MAA). Required: BA/BS in a scientific/health discipline, minimum 7 years industry experience (at least 5 years in regulatory or regulatory program management), and hands-on experience with eCTD, Veeva RIM, Smartsheet, and advanced PowerPoint.

The Manager, Project Planner at Parexel (Canada, remote) partners with Asset PMs and cross-functional teams to develop and maintain integrated project schedules and resource forecasts for clinical development, regulatory submissions, and selected commercial launch plans. Responsibilities include schedule/resource monitoring, scenario planning, risk identification, reporting/visualization (OnePager, Business Objects, Spotfire), and contributing to process improvements. Requires a bachelor’s or master’s plus experience; minimum 3 years project planning/management and at least 3 years applicable pharmaceutical or similar industry experience.

The Director, RWD Strategy – Europe will lead identification and acquisition of real-world scientific data, manage vendor and provider relationships, develop client-facing RWD strategy materials and proposals, ensure data governance and compliance, and partner with internal teams and regulators to apply RWD/RWE across clinical and commercial use cases. Requires 10+ years' industry experience and advanced degree in a related field.

Accountable for end-to-end RFP and contract processes including analyzing RFPs, coordinating SMEs, preparing proposals and budgets, obtaining third-party quotes, developing and negotiating contracts, establishing account-specific contract standards, and tracking KPIs. Requires 4+ years in proposals/contracts within a CRO or similar environment and fluency in English.

Parexel is hiring a Senior Regulatory Affairs Associate to coordinate preparation, compilation and submission of new drug applications and lifecycle activities across assigned regions. Responsibilities include submission planning, stakeholder coordination (RRL, LRR, RPR, SMEs), drafting M1 documents, labeling support, maintaining submission records (including Veeva and archiving systems), and tracking non-eCTD and eCTD submissions. Role requires a life sciences degree, 3+ years regulatory affairs experience in pharma/biotech, and fluent English.