- 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 Masters 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.
Remote Work :
No
Employment Type :
Full-time
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...
- 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 Masters 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.
Remote Work :
No
Employment Type :
Full-time
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