Lead the engineering team owning the shared technical foundation for AI delivery across Parexel. Responsibilities include defining AI platform strategy and architecture, ensuring reliability/observability for AI workloads, managing AI-specific vendors and contracts, leading incident response and continuous improvement, and partnering with Engineering, Quality, and Compliance for audit readiness. Requires a Bachelor's in a technical field, 10+ years in platform/data/AI infrastructure roles, production experience with AI platforms (GenAI runtimes, vector DBs, agent orchestration, MLOps), and experience with cloud platforms (AWS or Azure). Familiarity with life sciences or GxP-adjacent regulated environments is preferred.

The Global Study Manager II provides operational leadership and accountability for study management deliverables across the study lifecycle, including study start-up, monitoring, vendor/pCRO oversight, budgeting, TMF management, and inspection readiness. Role requires fluency in English, experience in clinical research/study management (6–7+ years depending on degree), ability to travel as required, and supports remote work in Argentina, Brazil, and Mexico.

Responsible for direct site-facing contract and budget negotiations through execution for assigned investigator sites, managing the Per-Subject Cost (PSC) process, and handling budget and non-legal escalations from ICLs or pCROs. The role leads other negotiators on assigned studies and collaborates with Legal, Finance, pCROs, invoicing specialists, and other stakeholders, while maintaining compliance with Parexel processes and ICH-GCP.

The Manager, Business Intelligence and Operations will design, maintain, and enhance Power BI dashboards and reporting solutions, own reporting lifecycle and data governance, analyze operational performance to identify trends and improvement opportunities, and partner with stakeholders to deliver executive-ready insights. Requires a bachelor’s degree, 5–8 years relevant experience, strong Power BI and Excel skills, and experience supporting senior leaders in a matrixed environment.

Parexel seeks a General Manager, FSP Operations to lead a strategic customer relationship, overseeing operational delivery, resourcing, quality, and financial targets across an FSP portfolio. The role requires 10+ years of leadership in CRO/pharmaceutical/FSP environments, strong financial and people management skills, experience with clinical operations and research technologies, and responsibility for account growth, governance, and executive-level client engagement.

Parexel seeks a Senior Medical Writer to author and review clinical and regulatory documents (protocols, CSRs, IBs, ICFs, clinical overviews/summaries, safety reports, CTD documents). The role requires ensuring compliance with ICH-GCP, FDA and EMA guidelines, coordinating cross-functional reviews, reviewing statistical outputs, performing quality checks, and mentoring junior writers. Candidates should hold a relevant degree (BSc/MSc/PharmD/MD/PhD or equivalent) and have medical writing experience in a CRO, pharmaceutical, or biotechnology environment; proficiency in MS Word/Excel and document management/collaborative authoring tools is required.

Parexel seeks a Senior Project Leader for Real-World Evidence (RWE) clinical trials to lead global study teams and manage day-to-day operations, scheduling, resources and budgets. Candidate should have 3+ years leading global clinical trials (CRO/Biotech/Pharma preferred), experience with regulatory submissions, strong problem solving, organizational and interpersonal skills. Role is homebased in the United States.

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.

Parexel is hiring a Senior Medical Writer (UK or Ireland, remote) to deliver and manage clinical documents for a functional service provider program. Responsibilities include drafting CTRs, CTPs, IBs and updates, managing EDMS and review cycles, conducting QC and publishing support. Requires a scientific degree, strong communication and 5 years' medical writing experience with knowledge of ICH GCP and clinical trial processes.

Parexel seeks a Senior Medical Writer to join a sponsor-dedicated team working remotely in Italy. Responsibilities include drafting and finalizing clinical documents (CTRs, CTPs, IBs, amendments, biomarker and submission materials), EDMS document management, SAP review, QC reviews, timeline management, and meeting preparation. Requires a scientific degree, strong communication and collaboration skills, and at least 5 years' medical writing experience with knowledge of ICH GCP and regulatory/clinical trial processes.

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 seeks a Senior Medical Writer to author, edit, and manage clinical and regulatory documents (e.g., protocols, clinical study reports, CTD sections, investigator brochures, informed consents). The role includes quality control, project/document management, collaboration with cross-functional teams, and adherence to SOPs and regulatory guidelines (e.g., FDA/EMA, ICH-GCP). Requires a Bachelor's in life/health sciences and fluency in English.

Senior leadership role responsible for driving AI adoption and integration across the enterprise by translating technical AI and generative AI concepts for non-technical audiences, partnering with change management, learning and development, and corporate communications, and leading a team that curates education programming and strategic communications. Requires 10+ years of relevant experience and a bachelor’s degree.

Parexel is hiring a Senior Director to lead light-track delivery and AI automation (RPA, AI agents/assistants, citizen-developer enablement) in a remote capacity across the US and Canada. The role manages a portfolio of small-to-medium automation initiatives, establishes governance and reusable patterns, oversees UiPath-based RPA and agent development (e.g., Copilot Studio, PAIA), and leads multidisciplinary distributed teams. Required: bachelor’s degree, 12+ years in technology delivery/automation leadership, and at least 5 years leading multidisciplinary teams; experience in regulated/life-sciences environments is valued.

Responsible for planning and managing UAT deliverables, creating and executing test scenarios/scripts, coordinating testers and vendors, and ensuring validated eClinical systems meet sponsor and regulatory expectations. Requires 5+ years in clinical research/CRO or related settings, experience with clinical trial systems configuration/validation, and fluency in English.

Parexel is hiring a Senior Project Leader to manage medium-to-high complexity clinical trials remotely from India. The role requires 10+ years in clinical research or regulated environments, strong project management and strategic skills, knowledge of ICH-GCP and standard clinical systems (CTMS, EDC, IXRS, TMF), and responsibilities include project planning, budget and risk management, client relationship ownership, team leadership, and external representation.

Parexel is hiring a Senior Real-World Evidence (RWE) Programmer to work remotely from Canada or the continental United States. The role is highly hands-on (80–90% coding) and focuses on designing and coding R and SQL programs, cleaning and validating RWD from sources such as Flatiron and Optum, building data solutions on Snowflake, applying epidemiological and advanced statistical methods (time-to-event, longitudinal, cross-sectional), and producing dashboards, reports and reproducible documentation. Requires an MS in a related field, fluency in R and SQL, hands-on Flatiron experience, and at least 2–3 years of RWD/RWE experience.

Parexel is hiring a Biostatistician II to lead and execute statistical aspects of clinical studies of low to moderate complexity, contribute to protocol and analysis plan development, perform statistical analyses and quality control, and support regulatory submissions. Required: Master's + 3 years industry experience or PhD + 1 year; experience with clinical trials and statistical analysis; experience or skills in SAS or R; strong English communication and teamwork skills.

Parexel is hiring a Clinical Research Associate II/Senior for a home-based (Argentina-remote) role, with preference for candidates in Buenos Aires. Requires a bachelor’s in life sciences/pharmacy/nursing (or related), fluency in English and Spanish, a valid driver’s license, and a minimum of 1 year CRA experience. Responsibilities include monitoring sites (on-site and remote), managing site study documentation and visit reports, maintaining investigator relations, implementing corrective actions, and ensuring sites are inspection-ready.

Parexel seeks Project Leader and Senior Project Leader candidates for its Biotech division to lead global clinical trials (including Respiratory). Responsibilities include leading project teams, managing day-to-day operations, project scheduling, resource and budget management, coordinating team activities, and supporting the full clinical development process through regulatory submissions. Requires an undergraduate degree in a clinical/health field (advanced degree preferred) and at least 2 years' experience leading global clinical trials (CRO, biotech or pharma preferred). Role is home-based in the United States.