The role is a remote Senior Project Specialist based in Poland or Romania responsible for coordinating and finalizing documentation and approvals for scientific leader engagements (CSAs), managing document repositories, aligning logistics with vendors and scientific leaders, overseeing vendors/agencies, and ensuring compliance. Requires 3–5 years supporting medical affairs/KOL engagement, experience with Veeva Vault, contracting knowledge, and strong English communication skills. Occasional travel (10–20%) is required.

Senior Pricing and Market Access Consultant role requiring a minimum of 6 years' experience (including at least 3 years project management) to lead development of pricing and market access materials (eg, global value dossiers, HTA submissions), manage client relationships and mentor project teams. Locations listed include Spain, Poland, Italy, Romania and the United Kingdom (remote and office-based options).

Responsible for coordinating design, planning and execution of early-phase clinical trials, providing clinical oversight, risk assessment, on-site monitoring and management of CROs. Requires experience with CTMS/TMF, protocol and clinical document authoring, knowledge of ICH-GCP and regulatory requirements; education options include Bachelor's (≥7 years), Master's (≥5 years) or PhD (≥1 year) in life sciences.

Provide tactical sourcing solutions and supplier coordination for depots, investigational medicinal products, couriers, and ancillary supplies to support clinical study execution. Responsibilities include supplier selection, contracting, commodity research, ensuring regulatory and local compliance, managing sourcing help desk tickets, creating and executing Statements of Work, handling import/export documentation, resolving supplier quality issues, and mentoring junior team members. Requires operational understanding of clinical studies and supply chains, knowledge of GCP/GDP, strong Microsoft Office skills, and analytical/problem-solving capabilities (preferred 4+ years sourcing/procurement experience in CRO or pharmaceutical environment).

Parexel seeks a Project Leader to manage clinical trials remotely from Hyderabad, India. Responsibilities include developing project plans, managing budgets and profitability, owning study-level client relationships, overseeing regulatory compliance (ICH-GCP), leading cross-functional teams, identifying and mitigating risks, and ensuring quality. Requires a bachelor's in a science/medical field and 10+ years' clinical research/project management experience; PMP and advanced degree are preferred.

Parexel is hiring a remote Site Activation Leader (Study Start‑Up Lead) to lead site activation planning and execution across multiple clinical studies. The role includes developing and managing study critical path plans, coordinating feasibility, site selection, regulatory and ethics submissions, TMF management, system setups (CTMS/EDC/IRT), monitoring activation progress, mitigating risks, guiding site activation teams, and supporting client communications and proposals. Requires a bachelor's degree and 4–7 years' clinical research operations experience with site activation leadership.

Parexel is hiring a Senior Patient Safety Project Lead (remote, must be living in Ireland) to manage end-to-end patient safety projects, provide cross-functional leadership, oversee budgets and scope, ensure regulatory and GxP compliance, support clinical adjudication and data monitoring committees, and act as primary client liaison. Requires strong pharmacovigilance and project management experience and fluent English.

Lead and manage day-to-day operations of global clinical trials for biotech clients (Dermatology and other therapeutic areas), including project scheduling, resource and budget management, coordination of team activities, and support through the full clinical development process and regulatory submissions. Requires an undergraduate degree in a clinical/health field (advanced degree preferred) and a minimum of 2 years' experience leading global clinical trials in project management within a CRO, biotech, or pharma company.

The Site Payment Lead manages end-to-end site/investigator payments for assigned studies in a remote capacity (Argentina). Responsibilities include payment setup and modifications, coordinating with project teams and internal stakeholders, ensuring timely and compliant payments, resolving escalations, participating in study start-up and strategy meetings, and producing payment reports. Requires a bachelor's degree, advanced English, and preferred 4+ years' experience in CRO, finance/accounting, or related roles.

Parexel is recruiting an experienced Clinical Project Leader or Senior Project Leader to lead global project delivery for Large Pharma Partnership clients. The role requires demonstrable CRO project leadership across Phase I–III clinical trials, strong financial and client relationship skills, oncology expertise (essential) and familiarity with ICH/GCP and eClinical systems. The position is available remote in specified countries (EMEA and South Africa).

Parexel Consulting (regulatory) is hiring a (Senior) Project Manager to act as client-facing lead for regulatory submission projects (PMDA consultation, CTD support, KOL engagement) from initiation to completion. Responsibilities include scope and budget confirmation, schedule and resource management, coordination of PMDA meetings, vendor and interpreter liaison, training setup, and reporting to an overseas (Europe) manager. English communication skills and project management experience are required; pharmaceutical industry experience is desirable.

Lead and develop a Production Services team responsible for clinical trial supply packaging, labeling, manufacturing support, production planning, and batch documentation. Ensure GMP/GDP and regulatory compliance, drive operational excellence and continuous improvement, manage supplier and quality activities (audits, CAPA), and partner with global cross-functional teams. Requires ~6+ years' experience in clinical trial supply chain or regulated pharmaceutical operations and fluent English.

Parexel seeks a Manager, Site Payment Services to lead and mentor a global team managing end-to-end site payments, fund setup, and investigator invoice payments. The role emphasizes operational excellence, process improvement, compliance, reporting, and stakeholder collaboration. Requires a minimum of 7 years' relevant experience and advanced English.

Parexel seeks a Senior Clinical Operations Manager to oversee project delivery and team performance for clinical trials. Responsibilities include monitoring project performance, resourcing, staff development, client/account management, quality control and ensuring compliance with ICH/GCP and SOPs. Requires substantial monitoring or data management experience or equivalent clinical research experience and a degree or clinical qualification. Competent in written and oral English and the local language; travel as needed.

Accountable for global execution of site activation and country start-up strategy for assigned clinical trials. Responsibilities include developing site start-up strategy, CRO and vendor oversight, regulatory submission support, TMF/CTMS documentation, metrics tracking, risk mitigation, and cross-functional leadership. Role may require up to 25% travel and requires 4+ years' relevant experience.

Experienced regulatory project manager role supporting Global Regulatory Leads to develop and execute globally aligned regulatory strategies and plans (IND/BLA/MAA), manage submission readiness (eCTD, Veeva RIM), facilitate Global Regulatory Subteam (GRST) meetings, and drive cross-functional alignment. Requires a scientific/healthcare degree, minimum 7 years industry experience (≥5 years in regulatory or regulatory program management), hands-on submission experience, and strong project management and communication skills.

Parexel is hiring project management professionals for its Biotech Division to lead global clinical trials in Neurology, Psychiatry and Rare Disease. Roles include Project Leader, Senior Project Leader and Project Director; candidates should have a minimum of 2+ years leading global clinical trials (CRO/biotech/pharma preferred) and experience in scheduling, resource and budget management, team coordination and regulatory submissions.

Parexel seeks Project Leader and Senior Project Leader candidates to lead Metabolic / GLP-1 / Obesity global clinical studies. Roles involve leading project teams, managing day-to-day operations, project scheduling, resources and budgets, coordinating team activities, and supporting the full clinical development process through regulatory submissions. Minimum requirement: undergraduate degree in a clinical/health field (advanced degree preferred) and at least 2 years' experience leading global clinical trials in a CRO, biotech, or pharma setting.

Deliver medical support and medical monitoring activities for clinical studies (including medical review of data, safety/serious adverse event review, medical input to PV workflows and regulatory safety reporting). Participate in study planning, protocol and study document development, training of study teams, audits/inspections, rotas for emergency medical contact, client engagement and support business development/proposal activities. Requires medical qualification, clinical practice experience, knowledge of GCP/ICH/FDA/EMEA guidelines and a minimum of 3 years' medical monitoring or medical data review experience.

Parexel seeks project leadership professionals to lead day-to-day operations of global clinical trials for biotech clients (including Oncology/Hematology), with responsibilities in project scheduling, resource and budget management, team coordination, and support across the clinical development process through regulatory submissions. Minimum stated requirement: 2+ years leading global clinical trials in project management.