You are responsible for managing biomarker studies as part of clinical trials according to the
You carry out consultations and provide operational input into quotes/proposals to ensure
You check the scope of work and budget accurately to achieve client expectations at all times
You define project milestones and check project performance against protocol, from signed contract
You control if the project is conducted in accordance with set global standards and procedures
You control the budget of assigned studies

🎯 Requirements

You have at least a Master’s degree in Biochemistry/ Life Sciences or a Bachelor degree in
You have experience with G(C)LP
You have a relevant regulatory biomarker experience with a CRO or pharmaceutical company
You have a strong customer focus
You have bioanalytical skills
You have excellent communication and interpersonal skills

🎁 Benefits

Do you meet the above profile and are you interested in an informal and pleasant working

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