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We are expanding in our team working with integrations and are looking for a new GCP advisor specialist in the Clinical Compliance department, in R&D Quality Do you dream of using your GCP knowledge, clinical research experience and perhaps GCP audit experience and last but not least your quality mind-set in a highly professional and engaged global environment? Have you worked with clinical quality, and will you bring a ‘can-do’ attitude to support high quality in the development of innovative treatments for patients? Then you could become our new GCP Advisor Specialist. The position
As a GCP Advisor Specialist in our Integrations team, you will have the opportunity to:

Support and ensure a smooth and well-integrated process of acquired assets into our organization.

Shape and optimize the framework for the clinical quality role in integrations.

Take ownership and responsibility for contributing to the right quality level in the global organization.

You may also be involved in improvement/optimization projects, act as a quality partner for key projects/lines of business, and provide GCP advice to stakeholders. Qualifications
To be successful in this role, we are looking for someone with the following qualifications:

A degree in pharmacy, medicine, science, or a similar field

At least 5 years of experience in clinical research and drug development

Solid knowledge of GCP and other relevant r...