Clinical Research Trials Assistant

About the Role

Core Responsibilities Develop knowledge of the ethical principles for clinical research and its implications for current

practice. As a member of the R&D team, s/he will be responsible for the provision of robust operational support in all

aspects of clinical trials administration according to Good Clinical Practice (GCP) guidelines, local standard operating

procedures (SOPs) and other relevant SWLStG policies. Be responsible for his/her own personal and professional

development, ensuring that all relevant skills and training (e.g. GCP) remaining up-to-date to carry out all job-related

responsibilities. Help to identify mental health service users and carers who are eligible to take part in a range of

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.