Parexel is recruiting a Global Therapeutic Area Lead, Nephrology (Senior Medical Director) to provide medical oversight and clinical leadership across nephrology clinical trials. The role includes medical monitoring, development/review of protocols and safety documents, pharmacovigilance support, client engagement, mentoring, and participation in business development. Requires an MD (or equivalent), at least 10 years of clinical medicine experience with a nephrology specialty, and strong knowledge of ICH-GCP and drug development processes.

Parexel is hiring Global Study Manager II (GSM II) to lead and coordinate global clinical trial execution, including study start-up through database release, oversight of pCROs and vendors, site management, budgeting, inspection readiness and delivery against study plans. Role requires strong study management experience, CRO/vendor oversight, knowledge of GCP and the ability to travel as required. Located remotely in Mexico, Brazil or Argentina.

Parexel FSP seeks Clinical Data Managers (remote: Canada, Argentina, Brazil, Mexico) with 5+ years' data management experience for FDA-regulated clinical trials. Responsibilities include eCRF/EDC design and testing, edit checks, query and SAE reconciliation, vendor/CRO coordination, UAT, database lock activities, and contribution to DMPs and SOPs. Strong English communication and knowledge of CDISC, ICH-GCP, 21 CFR 11, MedDRA expected.

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.

Lead clinical operations in the Czech Republic as Country Head/Director: oversee managers and senior contributors, ensure on-time high-quality project delivery, manage resourcing and staff development, support business development and client engagement, maintain compliance with ICH/GCP and company SOPs. Requires fluent Czech and English and substantial management experience in clinical research; degree in a health-related discipline or equivalent clinical experience preferred.

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.

Provide regulatory affairs services with emphasis on Clinical Trial Applications (Phase I-IV) across multiple therapeutic areas. Responsibilities include project execution and planning, client interactions, consulting, quality documentation and CMC-related activities. Preferred experience includes early phase studies and work involving medical devices, GMOs, radiopharmaceuticals and biological drugs. Role requires several years' industry experience and a scientific/technical degree.

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.

The Executive Director, Global Site Payment Strategy & Services will lead a global organization responsible for investigator payment operations across regions and therapeutic areas. The role focuses on strategy, operational excellence, process improvement, automation, analytics and AI, stakeholder engagement with Finance/Technology/Operations, and development of a high-performing global team. Requires 10+ years of progressive leadership experience in pharmaceutical/biotech/CRO or healthcare services and deep knowledge of investigator financial operations.

Accountable for defining strategy and operating model for global investigator payment operations; leading a distributed team to deliver timely, compliant payments, implement automation and AI-enabled solutions, and partner with Finance, Technology, Operations and Commercial stakeholders to improve site experience and operational scalability. Requires 10+ years of progressive leadership in pharmaceutical/CRO/healthcare services and deep expertise in investigator financial operations.

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 is hiring a Senior Regulatory Affairs Consultant (CTA) to support clinical trial application (CTA) submissions for Parexel and clients across European locations. The role involves managing regulatory activities and deliverables for CTA submissions, compiling core submission packages, authoring documentation, leading and contributing to global team efforts, and liaising with regional/local partners and Health Authorities. Requirements include a Bachelor's degree in a scientific/technical discipline, extensive CRO/pharma regulatory experience, client-focused approach, strong written and verbal communication (English and local language), and problem-solving skills. The position can be home- or office-based in Warsaw. Salary benchmarking provided: 235,656–353,484 PLN gross per annum.

Parexel seeks a Regulatory Affairs Consultant with several years' CRO/pharma experience in CTA submissions across European locations. The role involves leading and contributing to CTA compilation and authoring, coordinating global submission activities, working with study teams and health authorities, and performing in a client-facing capacity with support from senior staff. Position is home or office-based in Warsaw; salary range provided: 172,296–258,444 PLN gross per year.

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 end-to-end study management activities (startup through database release), providing leadership for recruitment, monitoring, vendor oversight and inspection readiness. Requires advanced clinical research/study management experience, proven CRO/vendor oversight, budgeting and familiarity with GCP; fluency in English and ability to travel as required.

Accountable for country and regional study operational delivery from startup through close, including site activation, recruitment strategy, CRO and vendor oversight, regulatory/ethics submission coordination, quality and risk management, and escalation resolution. Requires a scientific/technical degree and 3–5 years relevant operational clinical trial experience depending on degree.

Parexel seeks a Medical Writer II / Senior Medical Writer to develop and finalize clinical and regulatory documents (CTRs, CTPs, IBs, protocol amendments, biomarker reports, submission documents), manage documents in EDMS, coordinate review cycles, perform quality control, and support publishing and approval processes. Role is remote for Spain and Poland; minimum one year of medical writing experience required.