Teams at Parexel

The Senior Regulatory Consultant will oversee regulatory strategies, manage complex timelines, enhance team performance, and guide regulatory projects to support the development of transformative therapies.

The Senior Clinical Research Associate manages monitoring and site activities for oncology trials, ensuring compliance with protocols and regulations while collaborating with clinical study teams and site personnel.

Provide operational and administrative support for clinical trials from start-up to closeout, including maintaining TMF and CTMS, tracking trainings and supplies, preparing meeting documentation, performing quality checks, supporting study teams and vendors, and assisting with basic financial tracking.