Analytical Project Manager

Job description

You are responsible for managing biomarker studies as part of clinical trials according to the regulatory requirements; You carry out consultations and provide operational input into quotes/proposals to ensure capabilities and client needs are aligned; 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 to invoice paid; You control if the project is conducted in accordance with set global standards and procedures; You control the budget of assigned studies; You complete and accurate study files to pass prevailing regulatory inspections; You support sponsor and internal audits. You have at least a Master’s degree in Biochemistry/ Life Sciences or a Bachelor degree in Biochemistry/Life sciences along with significant industry experience; 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; You are good at establishing and maintaining internal and external relationships; You are energetic and enthusiastic with a flexible and dynamic work ethic; You have an excellent command of Dutch and English, spoken and written.