Clinical Research Nurse/ Practitioner

About the Role

Clinical Trial Management (CTIMPs and Non-CTIMPs) Obtain informed consent from participants for non-CTIMP studies (i.e.

observational and questionnaire) as instructed by Principal Investigator (PI) and within parameters of the protocol.

Support participants considering taking part in interventional and observational research with the decision-making

process, ensuring that their information needs are met sensitively and that they have a full understanding of the

research study and its requirements. To ensure all Adverse Events are reported in line with the Trust Adverse Events

Reporting policy Ensuring all reporting to regulatory bodies and Research Networks (if applicable) is done in a timely

Responsibilities

• Perform core duties as described.

Requirements

• Relevant experience or willingness to learn.

Benefits

• Benefits per job description.

Compensation

To be discussed.

Location & Schedule

Per job description.

How to Apply

Use the “Apply” button.