Jobs at Parexel

The Training Development Lead will oversee the design, development, and implementation of global training courses in clinical research and regulation, managing deliverables and stakeholder communication while ensuring compliance with educational standards.

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.

Conduct site monitoring visits, manage site relationships, ensure compliance with protocols, and evaluate trial data integrity in clinical research.

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.

Senior leader accountable for coordinating and aligning data products across clinical, corporate, and commercial domains. Leads a team of Data Product Coordinators, manages intake/prioritization, drives cross-functional delivery across data ingestion, engineering and distribution, and establishes governance, KPIs, operating models, and stakeholder alignment in a matrixed global CRO environment.

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.