Job Description
We are currently working with a pharma organisation who are a growing ecosystem of drug development companies, that provide integrated and specialist operational support for rapidly scaling biotech ventures.
They are looking for a GCP QA Manager who will work closely with the Head of Quality and Clinical Teams to advise and oversee GCP compliance in accordance with local and international quality standards.
The role will include review and approval of GCP quality documents such as SOPs, Policies, Forms, and other key essential documents supporting clinical trials.
This is a 6M day rate opportunity with hybrid working based near Oxford.
The expectation to be on site is 1 or 2 days a week.
You must be available to start ASAP.