Clinical Trial Associate

Clinical Trial Associate focuses on involve delivering clinical research work to a high standard, working closely with your team and stakeholders.

What the role involves

• Involve delivering clinical research work to a high standard, working closely with your team and stakeholders.
• Assisting in the coordination and administration of clinical trials, ensuring compliance with protocols and regulatory requirements.
• Maintaining and organize clinical trial documentation, including study files, essential documents, and regulatory submissions.
• Supporting the preparation of study-related materials, such as informed consent forms and case report forms.
• Ensure smooth trial execution.
• Contribute to the tracking and reporting of clinical trial metrics and milestones.

Skills and requirements

• Bachelor's degree in a scientific or healthcare-related field.
• Prior experience or strong interest in clinical research.
• Knowledge of clinical trial processes, regulations, and guidelines.
• Willingness to travel as required (approximately 10%).

Confirmed role details

• Clinical Trial Associate - hybrid working.
• A range of health insurance offerings to suit you and your family’s needs.
• Plan with confidence for the years ahead.
• Competitive retirement planning offerings to maximize savings.

Candidate fit

• clinical judgement, NMC standards, calm communication, and careful documentation