Liver Research Data Manager

About the Role

1. Clinical Responsibilities Responsible for accurate completion of Case Report Forms (CRFs). Responsible for the

collection, co-ordination and computerisation of data generated from the clinical trials. Implement and adhere to the

principles of GCP (Good Clinical Practice) as set out in the Clinical Trials Regulations. Act as a resource and support

to patients and their relatives, explaining practical aspects of clinical trials, assisting and supporting nursing

teams. Act as a resource for liver based research. Work in accordance with all regulatory requirements including: -

Local Standard Operating Procedures (SOPs) - Good Clinical Practice - Medicines for Human Use (Clinical Trials)

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.