Responsible for managing clinical operations aspects of studies including study start-up, site selection, monitoring oversight, TMF quality, vendor coordination, recruitment/retention monitoring, risk management, audits/inspections and cross-functional liaison. Ensures compliance with ICH-GCP, SOPs and study procedures and provides leadership to virtual project teams.

Senior role leading risk management, audit/inspection readiness, QREs, RCA/CAPA and quality oversight across projects and accounts. Requires 8-12 years' clinical research experience, fluency in English, deep knowledge of ICH-GCP and experience mentoring teams; role is remote (South Korea) with ~15-20% travel.

Parexel FSP seeks a Senior Clinical Research Associate to manage site-level activities from activation through database lock, ensuring compliance with ICH/GCP and applicable regulations. The role includes monitoring AEs/SAEs, interfacing with study teams and vendors, supporting audits and CAPA, and is sponsor-dedicated with preferred oncology experience. Minimum ~3.5 years site monitoring experience is required.

Parexel seeks a Senior Associate/Consultant to provide CMC regulatory strategy and submission support for biologics and vaccines. Responsibilities include authoring/reviewing Modules 1–3, performing gap analyses, managing global submissions (US, EU, international), and partnering with Regulatory, Quality, and Manufacturing stakeholders. Requires hands-on experience with commercial biologics/vaccines and strong knowledge of FDA/EMA requirements; Veeva Vault experience is a plus.

Parexel is hiring a General Ledger (GL) Accountant to work remotely from anywhere in Argentina supporting LATAM entities. Core responsibilities: prepare and maintain GL journal entries, own month-end close activities, prepare and analyze balance sheet reconciliations, support statutory financial statements and GAAP reconciliations, manage intercompany transactions, assist with audits and tax filings. Required: bachelor’s in accounting or related field, 1–2 years in accounting/Record-to-Report, advanced Excel, experience with ERP systems (Oracle preferred), advanced English; knowledge of US GAAP is a plus.

Serve as Global Submission Coordinator for EU and US, coordinating preparation, compilation, and submission of new drug applications and lifecycle activities. Responsibilities include organizing submission teams, preparing Submission Content Plans, drafting M1 documents, supporting labeling and artwork processes, managing non-eCTD dispatch and archiving, updating Veeva, and liaising with CMC, regional and local regulatory representatives and subject matter experts. Role requires regulatory affairs experience in pharmaceutical/biotech, knowledge of EU and US submission processes, familiarity with submission routes (e.g., reliance pathways), and proficiency in regulatory tracking systems and Microsoft Office.

Responsible for monitoring and managing investigator sites (SDV, patient safety, issue identification and closure), training site staff, maintaining SMF/TMF/ELARA documentation, generating monitoring reports, and ensuring studies run per ICH/GCP, local laws and client SOPs. Requires degree in life sciences/nursing/pharmacy and clinical monitoring/site management experience.

The SUPM II is accountable for planning, coordinating and delivering site activations to plan for medium-to-large interventional studies or assigned regions/countries. Responsibilities include developing start up strategies, managing timelines in an enterprise project management system, coordinating regulatory submissions and site readiness activities, mitigating risks to site activation, and integrating protocol amendments. Required: fluency in English and at least 5 years' global study start up/clinical trial management experience; knowledge of GCP and clinical trial methodology.

Role involves designing and developing ETL mappings and workflows, building data warehouses and SQL solutions on Azure/Synapse/Databricks, implementing data quality and ETL testing (Informatica), and providing application support and technical consulting for clinical trials information-sharing solutions. The position includes producing technical and architectural artifacts, mentoring engineers, and supporting release management.

Parexel is registering interest for a UK-based, home-based Country Study Operations Manager to manage study and country-level activities from start-up through conduct and close. Responsibilities include implementing start-up and site activation plans, recruitment strategy, study-level planning support, vendor and budget management, and communication with local teams, CROs and stakeholders. Minimum 5 years' relevant clinical trial management experience and a university degree or nursing qualification are required; senior study start-up experience is preferred.

Parexel is registering interest for Senior CRAs for UK sponsor-dedicated roles. Candidates must have at least 4 years' CRO or pharma trial experience, oncology trial experience including RECIST, and fluency in English. The role involves virtual and occasional on-site monitoring per the Study Monitoring Plan, ensuring data integrity, ICH-GCP and protocol compliance, source document verification, CRF review, IP accountability, query resolution, adverse event follow-up, and site-level coordination and documentation.

Parexel seeks a Statistical Programmer II to produce and QC derived clinical trial datasets, tables, figures, and listings using SAS (including SDTM and ADaM). The role requires adherence to SOPs and regulations (ICH-GCP, 21 CFR Part 11), participation in project start-up and documentation, and providing training/mentorship as appropriate. Competent written and oral English and a relevant degree or equivalent experience are required.

Senior Manager responsible for strategy, operations, and financial management of Parexel’s global network environment, including SD-WAN, Palo Alto firewalls, Cisco/Meraki LAN/WLAN, telecom, and AV. Role includes vendor and contract management, budgeting and cost optimization, driving standardization, security and compliance alignment, capacity and resilience planning, incident escalation, and leading engineering and operations teams. Requires 10+ years progressive experience.

Lead RWD strategy and data access across selected European markets, developing client-facing proposal materials, executing regional RWD acquisition strategies, managing vendors and partnerships (EMR/EHR, claims, registries, specialty data), ensuring governance and ROI, and aligning RWD approaches with regulatory guidance such as EMA. Role requires senior hands-on RWD experience, cross-functional collaboration, and leadership.

Parexel is hiring for a Clinician / Clinician Manager in Shanghai and Beijing, China (remote indicated). The company works across clinical trials, regulatory, consulting, market access, and clinical development.

Parexel is registering interest for a Trial Vendor Senior Manager to independently manage vendor-related deliverables for global clinical trials (schedule, budget, quality/compliance). Responsibilities include vendor oversight, contract and budget review, UAT for eCOA/IRT, site readiness, risk mapping, and using tools such as Unified Vendor Portal, Clinical Insights and FIRST. Requires a bachelor's degree (advanced preferred), 3+ years' clinical operations/vendor management experience, knowledge of GxP/ICH, and proficiency in English.

Parexel seeks a Senior Consultative Sales Director for Emerging & Growth Accounts to drive new business acquisition, lead proposal strategy and pricing, manage client prospecting and relationships, and collaborate with Solutions Consultants and delivery teams. Role requires B2B CRO sales experience (selling phase II/III clinical services), strong consultative and analytical skills, and willingness to travel ~50%.

Responsible for defining and delivering global start-up strategy and site activation plans for medium to large interventional studies across regions. Duties include timeline planning in an EPM system, coordinating regulatory submissions and investigational product supply, risk mitigation, managing cross-functional start-up teams, implementing protocol amendments at sites, and driving process improvements. Requires extensive global start-up and clinical trial management experience and fluency in English.

The Study Start Up Project Manager (SUPM) is responsible for defining and delivering global start-up strategy and site activation plans for interventional clinical studies or assigned countries/regions. Responsibilities include coordinating regulatory submissions and start-up activities, managing timelines within an EPM system, assessing and mitigating risks to site activation, integrating protocol amendments, and leading start-up teams and meetings. Requires extensive start-up clinical trial experience, knowledge of GCP and clinical trial methodology, project management experience, and fluency in English. Education: BS/BA with 5 years relevant experience or MS/PhD with 3 years relevant experience.

Parexel Clinical Research Associate II supporting site performance and monitoring activities per monitoring plan and ICH-GCP. Responsibilities include SDV, drug accountability, SAE reporting, data query resolution, investigator/site training, preparation for audits/inspections, and maintaining essential study documentation. Requires minimum 2 years CRA experience and fluency in English and the host country language.