Jobs at Parexel

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.

Provide strategic HR business partnering across the UK and Ireland, advising managers on employee relations, performance, talent development, compliance, HR analytics, payroll validation, and organizational change. Coordinate global HR processes, support restructuring initiatives, deliver HR training, communicate policy updates, and develop people-focused solutions across regional client groups. The role is a 12-month fixed-term contract with hybrid work in London.

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.

Conducts on-site and remote monitoring of oncology clinical trial sites, ensuring protocol, ICH-GCP, regulatory, data quality, and patient safety compliance. Reviews source documents, medical records, consent documentation, CRF data, investigational product accountability, site logs, and protocol deviations. Resolves queries, tracks action items, documents monitoring activities, supports inspection readiness, and collaborates with investigators, site staff, Site Managers, and project teams to meet trial timelines.

The Senior Clinical Research Associate is responsible for ensuring data integrity and compliance with protocols in oncology trials, managing monitoring activities and collaborating with site personnel.

Leads clinical trial site delivery across preparation, initiation, monitoring, and closeout. Manages investigator relationships, protocol compliance, source data review, safety reporting, quality risk assessments, essential documents, study supplies, and issue escalation. Uses CTMS, eTMF, and remote monitoring tools while supporting audits, inspections, patient recruitment, and inspection readiness. Collaborates with cross-functional and global teams to ensure patient safety, regulatory compliance, accurate data, and high-quality study execution.

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.