Jobs at Parexel

The Workday Change Management Specialist focuses on driving effective technology adoption at Parexel through communication, training, and user support related to the Workday HCM platform.

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.

The Senior Clinical Research Associate will oversee compliance and data quality in oncology trials, coordinate site activities, and manage monitoring responsibilities while ensuring regulatory adherence and data integrity.

As the Principal IT Project Manager, you will oversee critical technology projects, ensuring delivery within scope, budget, and quality requirements while managing stakeholder communications and risks.

Manage all aspects of contracts, including negotiation and documentation. Serve as the primary client contact and ensure compliance throughout the project lifecycle.

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 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.

The Clinical Compliance Manager provides regulatory compliance support for clinical studies, ensures adherence to GCP guidelines, and manages compliance-related activities to mitigate risks.

The Senior Business Development Director will drive new business acquisition, maintain client relationships, and collaborate on strategic sales plans. Responsibilities include understanding client needs, ensuring effective proposal strategies, and influencing decision-makers to achieve sales goals in a competitive environment.

The Director RWD Strategy leads the implementation of real-world data initiatives in Europe, managing partnerships and proposal development while ensuring compliance with data use agreements.

The Manager, Central Monitoring will oversee centralized monitoring activities, analyze key data indicators, support clinical teams, and ensure data integrity in studies.

The Senior Clinical Study Administrator coordinates clinical study activities, manages documentation, supports regulatory submissions, and ensures compliance with protocols and standards.

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.

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.