Compliance Officer

The Clinical Research Unit Cambridge (CUC) is based on a hospital site and conducts phase 1 clinical studies. This role involves dealing with issues: organising investigation meetings, overseeing root cause analysis and corrective and preventative action planning, documentation and ensuring actions are completed on time. As part of a small quality team enabling the CUC to operate to the highest standards, you will offer advice on quality issues to a wide range of personnel. You will also be involved in maintaining policies and procedures, and support compliance training.

Good interpersonal skills are essential as you will interact with a variety of clinical/scientific teams, as well as the ability to conduct thorough investigations and ensure pragmatic solutions. You will have excellent attention to detail and written documentation skills, and be able to maintain and update databases. You must have knowledge of Good Clinical Practice and/or Good Manufacturing Practice, as well as ethics and regulatory requirements relating to clinical research and previous experience within a quality/compliance environment within the pharmaceutical industry. This position is for someone with GCP/GMP experience wanting a career in quality and compliance.

Salary negotiable depending on experience

Exacting safety standards in place