You will also have a chance to work on various therapeutic areas, expand on your existing knowledge and never be bored as there is a wide variety of products to work with.
The company is a medium sized global CRO that has combined the beauty of both worlds- not too small and not too large so there are a lot of opportunities in a stable and growing company with a lovely friendly culture.
You will manage day-to-day operations of the project according to ICH/ GCP guidelines and other relevant regulations, review and provide input study protocol, check specifications, final study report, manage site quality as well as supervise CRAs.
Please apply if you fulfil the following requirements:
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