Job Summary

• Fully conversant with the trial protocol, Case Report Forms (CRFs/eCRF), off-site manual (if applicable), supporting documents, procedures, and timelines to enable day to day running of the trial including all relevant SOPs.
• Communicate effectively with the Illingworth research nurse project manager (RNPM), Research nurse manager, site staff and the Principal Investigator, to ensure a smooth and efficient flow of information.
• We are passionate about developing our people, through career development and progression; career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program.

Matching Summary

Skills & Requirements

Key Requirements

• Registered nurse
• 2 years' post qualification experience
• Research and clinical trials experience
• GCP certification
• Venepuncture and ECG preferable
• Ability to work autonomously
• Excellent verbal and written communication skills
• Ability to prioritize and manage multiple tasks
• Good working knowledge of computer software

Work Rights