- 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.
Qualifications
- 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.
Additional Information
Do you meet the above profile and are you interested in an informal and pleasant working environment? We are looking forward to receive your CV and motivation letter.