Jobs at Parexel

Leads enterprise data engineering strategy and global teams responsible for real-world data movement, lakehouse architecture, ingestion, transformation, storage, optimization, governance, security, and standardized data products. Partners with technology, analytics, and business stakeholders across clinical, safety, financial, and corporate domains. Oversees delivery prioritization, roadmaps, quality, reliability, team development, and scalable cloud data solutions using Azure Databricks, SQL, Python, and CI/CD.

Oversee local clinical trial delivery from site identification through closeout, leading CRAs and CSAs, coordinating monitoring, regulatory submissions, budgets, risk management, essential documents, and investigator relationships. Ensure compliance with ICH-GCP and local regulations, support patient recruitment, resolve study issues, and perform site monitoring as needed. Requires clinical research experience, team leadership, project management, regulatory knowledge, and a life sciences degree.

Oversee oncology clinical trial monitoring across investigator sites, ensuring protocol compliance, patient safety, data integrity, informed consent, investigational product accountability, and regulatory readiness. Conduct remote and on-site monitoring, review source documentation and clinical data, manage deviations and queries, document findings, track site performance, and collaborate with investigators, sponsors, and project teams to support study delivery.

Leads pricing and market access consulting engagements for pharmaceutical and biotechnology clients. Advises on pricing, reimbursement, HTA, payer evidence, value communications, launch readiness, and market access strategy. Oversees project delivery, budgets, timelines, proposals, client relationships, and business development. Mentors consulting teams, develops thought leadership, and collaborates with clinical, regulatory, HEOR, RWE, medical, and commercialization experts across the product lifecycle.

Provides senior-level statistical programming expertise for clinical trials using SAS. Leads programming teams, produces and quality-controls SDTM and ADaM datasets, tables, figures, listings, and submission documentation. Coordinates timelines, budgets, resources, sponsors, and cross-functional stakeholders while ensuring compliance with SOPs, ICH-GCP, CDISC, 21 CFR Part 11, and regulatory standards. Also mentors staff, supports audits and inspections, and contributes to process improvement and technical consulting.

Leads global clinical trial projects for mid- and large-sized biopharma clients. Responsibilities include project planning, risk and quality management, budgeting and forecasting, client relationship management, cross-functional team leadership, invoicing, change-scope management, and bid defense support. The role requires strong CRO experience across Phase I–III trials, oncology expertise, clinical research knowledge, ICH GCP familiarity, financial management skills, and proficiency with Microsoft Office and clinical research systems.

Lead global clinical trial projects for large pharmaceutical partnership clients, overseeing cross-functional teams, project plans, budgets, risks, quality, timelines, client relationships, invoicing, and regulatory compliance. The role requires strong CRO experience across Phase I–III studies, oncology expertise, financial and client management, bid defense participation, and knowledge of ICH GCP and clinical research protocols.

Lead clinical operations FSP programs within a CRO, overseeing service delivery, client satisfaction, regulatory compliance, financial performance, resource allocation, workforce planning, quality metrics, and contract management. Develop scalable delivery models, standardize processes, improve margins, expand service offerings, and build strong cross-functional client and internal stakeholder relationships across therapeutic areas.

Lead complex international congresses and pharmaceutical meetings from planning through post-event analysis. Manage delegate travel, venues, suppliers, budgets, client relationships, compliance, deliverables, and on-site execution. Provide status updates, resolve issues, maintain quality and profitability, and support virtual meeting and registration technology. Requires event management experience in pharmaceutical, clinical research, or healthcare settings and a bachelor’s degree.

Leads commercial strategy, market positioning, competitive analysis, and high-impact bid pursuits for Parexel. Evaluates opportunities, guides RFI and RFP teams, develops persuasive sales messaging, prepares client presentations, analyzes wins and losses, monitors industry developments, and strengthens client relationships. The role collaborates globally across sales, operations, and technical teams to improve commercial effectiveness, increase pursuit win rates, and drive new business growth.

Leads Data Management Functional Service Provider programs within a CRO, overseeing service delivery, operational performance, financial management, workforce planning, regulatory compliance, client relationships, and scalable solution development. The role drives quality standards, reporting, process harmonization, resource optimization, profitability, and strategic growth across multiple therapeutic areas while managing cross-functional teams and stakeholder partnerships.

Lead a global organization delivering investigator payment services across regions and portfolios. Define strategy, drive operational excellence, modernization through automation and AI, partner with Finance/Technology/Operations, manage stakeholder escalations, and build high-performing global teams.

The Senior Clinical Research Associate will manage the operational aspects of clinical trials, ensuring compliance with regulations and monitoring sites to ensure patient safety and quality of studies.

The Executive Director leads HEOR Consulting projects, manages teams, ensures client satisfaction, and drives AI integration within healthcare solutions while overseeing business development and strategic planning.

The Project Leader/Senior Project Leader will oversee biotech projects, ensuring quality leadership, client satisfaction, and compliance with standards throughout clinical trials in various therapeutic areas.

The role involves designing clinical development programs, conducting statistical analyses, and ensuring evidence aligns with global strategies for Access and HTA needs.

The Senior Clinical Research Associate will ensure compliance with ICH GCP and local regulations, overseeing data integrity and conducting monitoring activities both remotely and on-site, particularly in oncology trials.