Responsible for end-to-end operational oversight of global clinical studies: sourcing and vendor selection, study startup, monitoring and TMF management, budget and contract oversight, CRO/vendor management, inspection readiness, and mentoring Study Operational Managers. Requires clinical research/study management experience and advanced knowledge of study management processes and GCP.

Parexel is hiring a Program Lead, FSP Operations (Data Management) to lead Data Management FSP programs. Responsibilities include strategic direction, financial management (budgeting, profitability, billing), workforce infrastructure and forecasting, quality and performance metrics, regulatory compliance, and stakeholder/client relationship management. Requires minimum 5+ years FSP Data Management leadership in a CRO and at least 3 years of line management experience.

Parexel is hiring a remote Data Manager Lead / Data Manager II to serve as the primary Data Management contact for assigned studies, manage study delivery timelines (Go-Live, interim deliveries, final database lock), collaborate with cross-functional teams globally, ensure compliance with ICH-GCP and SOPs, maintain inspection-ready Trial Master Files, identify and mitigate risks, support bid pursuits, and provide mentorship. Requires 6+ years hands-on clinical data management experience and familiarity with systems such as InForm, Rave, Veeva, and DataLabs. English fluency and ability to travel as required are stated.

Join Parexel's Clinical Trial Supply & Logistics team to execute study-specific supply chain strategies, manage inventory and sourcing, coordinate third-party providers, control Pass-Through Costs, and ensure compliance with GxP and ICH GCP. Role requires experience in pharmaceutical/clinical research or consulting, significant multinational experience, a relevant degree (or equivalent), and fluency in English.

Parexel is hiring a Clinical Vendor Manager (remote, UK or Ireland) to own vendor-related activities across the clinical trial lifecycle, ensuring service delivery, budget and contract oversight, quality/compliance with GxP and ICH, and performing UAT for eCOA and IRT. Requires minimum 5 years' experience in clinical operations and vendor management.

Parexel seeks a Regulatory Operations Submission Manager to plan, manage and track regulatory submissions (IND, DMF; CTA/NDA/BLA a plus) to global health authorities. Role includes submission strategy, eCTD expertise, project leadership, quality control, process improvement, and collaboration with CROs and cross-functional teams. Requires a life sciences degree and ~5+ years' regulatory operations/submissions experience.

100% home-based role in Poland supporting medical/scientific leader engagements under CSAs. Responsibilities include finalizing and maintaining engagement documentation, using internal processes and repositories (including Veeva Vault), coordinating logistics with vendors and scientific leaders, and ensuring compliance. Requires 3–5 years' administrative support experience in medical affairs, contracting knowledge, strong English communication, BA/BS degree, and intermittent travel (10–20%). Base pay range in Poland: PLN 160,000–175,000 per year.

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.

The Patient Compensation Lead will own processes and vendor oversight for participant compensation, reimbursement, and travel services. Responsibilities include implementing global payment and travel strategies, managing vendor performance, serving as a subject matter expert, coordinating with site payments and contracting teams, leading process improvements, and ensuring quality and compliance. Requires more than 8 years of relevant experience, a bachelor's degree (advanced degree preferred), clinical operations and payments experience, leadership and cross-functional collaboration skills.

Parexel seeks a Senior Regulatory Project Manager to partner with Global Regulatory Leads to shape and execute globally aligned regulatory strategies and plans across development and post‑marketing. Responsibilities include translating strategy into integrated plans, leading execution, facilitating Global Regulatory Subteam (GRST) meetings, managing timelines and risks, and preparing dashboards/reports for senior stakeholders. Requires a BA/BS in a scientific/healthcare discipline (advanced degree or PMP preferred), minimum 7 years industry experience (≥5 years in regulatory or regulatory program management), prior marketing application experience, and experience with eCTD, Veeva RIM, and Smartsheet.

Manager responsible for leading and mentoring a global team that handles end-to-end site payment management, ensuring timely fund setup and invoice payments, implementing process improvements, and producing regular reporting. Requires minimum 7 years' professional experience (CRO, finance/accounting or comparable) and at least 1 year of management experience; advanced English proficiency expected.

The Global Study Manager II provides operational leadership and accountability for study management, site management, pCRO and vendor deliverables across a study's lifecycle. Responsibilities include study start-up through database release, vendor and CRO oversight, budget and TMF oversight, inspection readiness, monitoring and enrollment oversight. Requires clinical research/study management experience, knowledge of GCP, and fluency in English.

Parexel seeks a Global Clinical Trial Leader (home-based in Austria) to manage planning, implementation, and oversight of international clinical trials, ensuring GCP and regulatory compliance, patient safety, data quality, vendor oversight, and timely delivery. Requires a degree (master's preferred) and a minimum of 5 years' clinical trial management experience; fluency in English is required. Preferred therapeutic experience includes Oncology, CNS, Immunology or Vaccines.

Parexel is hiring a remote-based Global Clinical Trial Leader in Germany to manage planning, implementation, and oversight of international clinical trials. The role includes trial feasibility, risk mitigation, vendor oversight, data delivery, safety reporting, TMF archiving, and cross-functional coordination. Requires a degree (master's preferred) and a minimum of 5 years' clinical trial management experience with knowledge of ICH-GCP and regulatory requirements.

Responsible for managing the life cycle of clinical site payment administration from startup through study close, including EDC-triggered visit payments, budget and contract configuration, vendor oversight, troubleshooting payment failures, ensuring purchase orders and funding, and supporting audit and cross-functional collaboration. Requires 2+ years relevant experience in clinical contracts/budgets, finance, or project/operations.

Lead the site contracting process for clinical trials including development of project setup documents and CTAs, managing contract cycle times and quality, advising on investigator grant budgets, providing leadership and training to site contracts teams, collaborating with stakeholders (sponsors, CROs, sites), and supporting cross-functional teams. Requires 5+ years of site contracting (or related CRO) experience and a bachelor's degree or equivalent.

Parexel seeks a Clinical Trial Leader (CTL) to plan, oversee and deliver assigned clinical trials (with preference for oncology and/or inflammation experience). The CTL leads trial teams, manages trial preparation, conduct and closeout (including feasibility, vendor oversight, patient recruitment, safety reporting, TMF and CTR delivery), coordinates with cross-functional and global stakeholders, and ensures compliance with GCP and applicable regulatory requirements.

Parexel seeks an Investigator Payments Lead, Associate to manage the lifecycle of clinical site payments from protocol mapping and budget configuration to EDC-driven visit payments and invoice processing. The role includes planning startup milestone payments, assessing EDC-to-budget mapping, troubleshooting payment issues, overseeing vendor adherence to payment processes, ensuring purchase orders and funding, supporting audit activities, and collaborating with clinical operations, finance, tax and legal. Location: Mexico-Remote and Argentina-Remote.

Parexel FSP is hiring Site Payments Associates (Argentina and Mexico, remote) to review clinical payment documents, extract payment information, configure budgets and payment lines in the Investigator Payment System (IPS), follow up on payee forms, escalate ambiguities, and track issues and resolutions. Requires fluent English, strong Excel skills, attention to detail, and basic clinical trial knowledge. BS degree or equivalent industry experience preferred.

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.