Senior role providing subject-matter expertise and technical leadership for statistical programming activities supporting clinical trials and regulatory submissions. Responsibilities include delivering and QCing derived datasets, tables/listings/figures, supporting CDISC standards and electronic submissions, mentoring staff, coordinating programming teams, and contributing to process improvements. Requires strong SAS skills and clinical trial experience; preferred 8+ years end-to-end programming with CDISC.

Remote Statistical Programmer II supporting clinical study data analysis and reporting. Responsibilities include producing and quality-checking derived datasets and TLFs, developing/using macros to improve efficiency, applying WSOPs and regulatory standards (ICH-GCP), maintaining study documentation, and collaborating with sponsors and cross-functional teams. Requires proficiency in SAS and clinical programming processes; a graduate degree is required. Preferred: 3+ years end-to-end programming (SDTM, ADaM, TLFs).

Parexel seeks a Global Trade Compliance Specialist to support clinical logistics in Latin America. Responsibilities include ensuring import/export activities comply with customs and government regulations, maintaining documentation, managing relationships with customs brokers and agencies, preparing and tracking import/export licenses, and designing compliance procedures. Requires experience in international trade within clinical trials or healthcare, working with global virtual teams, risk assessment and process improvement skills, proficiency with Microsoft Office, and fluent English. Role is remote (Argentina).

Join Parexel's Proposals and Contracts team as a Strategic Proposal Writer to lead proposal development from strategy through delivery. The role involves collaborating with proposal managers, sales leaders and cross-functional teams to produce differentiated, client-focused proposals and contracts, conducting market and therapeutic-area research, maintaining proposal templates, and mentoring junior staff. Experience in CRO proposals, FSP/FSO models, and strong proficiency in Microsoft Office and proposal-related tools is required.

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 seeks a Site Contract Lead / Senior Site Contract Lead to manage the full contracting lifecycle for clinical trial sites, including strategy, negotiation, execution, performance monitoring, and stakeholder communication. Role requires 3–8 years' relevant CRO or related experience (minimum 3 years), a bachelor's degree or equivalent experience, strong negotiation and contract management skills, proficiency with Office tools and contract management/eTMF systems, and the right to work and residence in one of the listed countries.

Provides quality oversight for technology solutions used in clinical trials, supporting computerized system validation (CSV), validation planning, risk assessment, change control, vendor audits and audit/inspection responses. Acts as a quality representative for the Parexel Quality System and supports development and continuous improvement of quality frameworks, training and compliance activities. Requires 2-3 years relevant experience and a degree in a related discipline.

Parexel seeks a Regulatory Affairs Consultant (Compliance & Process) to strengthen global regulatory compliance and quality operations across GxP environments. Responsibilities include controlled document management and governance, training governance, regulatory compliance and inspection readiness (FDA/EMA/MHRA), and management of QMS processes (deviations, CAPAs, change controls, SOPs). Requires a bachelor's in a related field, 8+ years' experience in regulatory compliance/QA within pharma/biotech, hands-on eDMS and Veeva Vault experience, and fluent English.

Parexel seeks a Director of Data Engineering (RWD) to lead strategy and hands-on engineering for the Enterprise Data Lake and lakehouse (medallion) architecture. The role requires 12+ years IT experience, strong expertise with Azure Databricks, SQL query tuning, Python, cloud data platforms, data ingestion/transformation, governance, and prior experience leading global data engineering teams in life sciences/real-world data contexts.

Parexel seeks a Senior Statistical Programmer to create SAS programs, produce derived analysis datasets and TLF content, perform programming validation, and support e-submissions. Requires a bachelor's in a relevant field, a minimum of 5 years clinical/statistical programming experience, proficiency in SAS, familiarity with CDISC (SDTM/ADaM), and experience with tools like XML and Pinnacle 21. Applicants must be authorized to work in Georgia, Poland, Serbia, or Hungary; the company cannot sponsor work visas.

Parexel is hiring a Client Relationship Director (remote, United States) to drive commercial growth, manage assigned accounts, lead bid pursuits and commercial negotiations, and collaborate with cross-functional teams. The role requires experience in pharmaceutical services/CRO or life sciences consulting, strong account management and strategic planning skills, and knowledge of clinical trial processes and related technologies.

Senior commercial leader responsible for leading commercial strategy initiatives, guiding high-impact RFI/RFP pursuits, conducting market and competitive analysis, and collaborating with sales, operations, and technical teams. Remote role supporting opportunities in Canada and the United States; requires 15+ years of CRO industry experience and willingness to travel as needed.

Parexel is hiring a Client Relationship Director to drive commercial growth, manage assigned accounts, lead bid pursuits and proposal strategy, and negotiate commercial contracts. The role requires experience in pharmaceutical services/CRO environments, demonstrated FSP sales experience, strong account management and commercial acumen, and a solid understanding of clinical trial processes and regulatory requirements. Bachelor's degree required; advanced degree preferred.

Parexel is hiring a remote Account Strategy Director (US or Canada) to serve as the strategic commercial and business-operations lead for mid and large biopharma accounts. Responsibilities include leading RFP/proposal strategies, developing customer intelligence and account plans, coordinating contract approvals, supporting business development and break-in strategies, and liaising across internal teams. Requires experience in life sciences/CRO environments, proposal and business development experience, familiarity with CRM and proposal tools, and strong communication and project management skills.

Parexel seeks a Regulatory Operations Technical Consultant to provide technical support, troubleshooting, validation, and client-facing consulting for regulatory publishing and RIM platforms (e.g., Veeva Vault RIM, Documentum, EXTEDO, Lorenz, Calyx). The role requires 3+ years' experience in regulatory operations/eCTD publishing, advanced Microsoft Office and Adobe Acrobat skills, system validation/testing experience, and fluent English. Candidates must be located in Mexico and work a fixed schedule (11:00 AM to 8:00 PM Mexico Time).

Join Parexel's Instructional Design team to design and develop high-quality, multi-modal training materials. Responsibilities include collaborating with SMEs and clients, applying instructional design methodologies and adult learning principles, ensuring visual and functional quality of deliverables, performing QA, and escalating/mitigating project risks. Role expects 2–4 years of relevant experience and strong graphic and technical writing skills.

The Initiation Clinical Research Associate (iCRA) leads and executes study start-up, pre-SIV, activation, and protocol amendment activities from site identification through activation. Responsibilities include managing regulatory and site documents, coordinating IRB/IEC and regulatory approvals, maintaining CTMS/eTMF/TMF documentation quality, supporting site readiness and training, and ensuring compliance with ICH-GCP, local regulations, sponsor requirements, and Parexel SOPs. Bachelor’s degree in a health-related field is preferred and excellent English (oral and written) is required.

Parexel is recruiting a Medical Writer II (referred to in the text as Senior Medical Writer) to prepare, coordinate, review, and finalize clinical and regulatory documents (including CTRs, CTPs, IBs, protocol amendments and submission documents). Responsibilities include EDMS document management, managing review cycles, quality control activities, stakeholder coordination, and support for publishing and electronic approvals. Location options mentioned are Hungary, the UK (Harrow/remote), or the Netherlands.

Parexel seeks a Senior Medical Writer to develop, coordinate, review, and finalize clinical and regulatory documents (e.g., clinical trial reports, protocols, Investigator's Brochures, biomarker reports) and manage document lifecycles within EDMS. The role involves driving review cycles, quality control, publishing activities, stakeholder coordination, and supporting submission-related documentation. Locations listed include Hungary, the United Kingdom, and the Netherlands (remote options noted).