Jobs at Parexel

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 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 Business Analyst collaborates with stakeholders to gather and analyze requirements, ensuring solutions align with regulatory standards and user needs.

Manage global clinical trials, oversee operational plans, ensure compliance with regulations, and lead cross-functional teams for trial success.

The Clinical Trial Manager will manage clinical trials, coordinate study materials, oversee monitoring activities, ensure regulatory compliance, and manage communication with vendors and research staff.

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 Senior Clinical Research Associate will lead clinical trials, ensuring adherence to protocols and regulatory requirements while contributing to the health improvement goals at Parexel.

The Project Manager leads Early Phase clinical trials, ensuring operational excellence, managing relationships with sponsors, and overseeing project execution across teams while mitigating risks and ensuring compliance with regulations.

The Senior Clinical Research Associate is responsible for monitoring clinical trial compliance, data integrity, data quality, and collaboration with site personnel to ensure regulatory standards are met in oncology trials.

The Senior Clinical Research Associate manages clinical sites, ensures compliance with regulations, trains staff, performs monitoring visits, and manages data quality during clinical trials.

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

The role involves supporting pharma and biotech clients in pricing and market access through data analysis, research, and strategic development, requiring strong communication and analytical skills.

As a Clinical Research Nurse, you'll administer investigational drugs, monitor participant safety, perform health assessments, and collaborate across departments in clinical trials.

Responsible for managing and monitoring assigned clinical trial sites, ensuring patient safety and quality execution from activation to database lock.

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.

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

The RoME Ecosystem Consultant will lead design and implementation of compliant ME&E ecosystems, focusing on finance and pharmaceutical compliance in a strategic partnership role.

The RoME Ecosystem Consultant will design and optimize the ME&E ecosystem, ensuring compliance and integration with software platforms, while coordinating efforts across various business functions.

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

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.