Senior Research Nurse

About the Role

Work autonomously to manage a large caseload of patients acting as a professional in ensuring a duty of care to the

patient and their families. Work within EU clinical trial directives in accordance with ICH GCP (International

Conference on Harmonisation and Good Clinical Practice) ensuring that the clinical trial protocol is adhered to at all

times. Identify patients suitable for entry into clinical trials by attending clinics (screening notes/consultant

referral) and Multidisciplinary Team (MDT) meetings. Participate in the informed consent process acting as a resource

and support to patients and their families Co ordinate the research patient pathway from screening through to trial

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.