Emerald Clinical Trials is a global leader in clinical research, partnering with biotechs and major pharmaceutical firms. The Clinical Trial Specialist (CTS) supports in-house site start-up and maintenance, ensuring trials meet regulatory standards and SOPs.
The CTS collaborates with project teams to manage feasibility, collect essential documents for site initiation, and assist with IRB submissions and ICFs changes, while maintaining high quality deliverables across TMF processes.
Global Clinical Trials Specialist - Start-Up & TMF employer: Emerald Clinical
Emerald Clinical Trials is an exceptional employer, dedicated to transforming clinical research while prioritising the wellbeing of both patients and employees. With a strong focus on purpose-driven work, competitive compensation, and flexible working arrangements, we foster a collaborative culture that values innovation and diverse perspectives. Join us in making a real impact on global health, with ample opportunities for career growth and development within a supportive environment.
