Eurofins Scientific is an international listed life sciences company that provides its customers with high-quality laboratory research and advice. Eurofins is a real start in bio-analytical testing for food, water, environment, cosmetics, pharmaceuticals and contract research for agroscience. In addition, Eurofins is one of the world's largest providers of testing and laboratory services in genomics, forensics, CDMO, advanced materials science, drug development and clinical studies. Eurofins uses a unique amount of analysis methods and an unprecedented high level of knowledge and expertise.

Eurofins consists of more than 50,000 employees worldwide, spread over 800 state-of-the-art laboratories and is active in 50 countries with a pro forma turnover of €5.4B in 2020. Eurofins has strong growth ambitions (CAGR 24%). In addition to very strong organic growth with many of its own start-ups, Eurofins also made a large number of acquisitions in various countries last year.

Our people at Euros make an important contribution to issues such as the environment, food and general health. Employees are proud of the work they do and experience a lot of freedom in the performance of the job. Responsibilities are as low as possible in the organization so that the people with the right information can start taking the right ones. Eurofins invests structurally in the personal development of talent, both in the field of leadership, growth potential and substantive knowledge.

Eurofins Central Laboratory is a dynamic, strong organization that offers laboratory services worldwide. supporting us the pharmaceutical and biotechnology industry with a full suite of central laboratory services. In addition, we provide extensive support in Biomarkers, Bioanalysis of Small and Large Molecules, Immunogenicity, Microbiology and Genomics. Our facilities are located in the US, Europe, Singapore, China and India.

The Study Director Assistant is responsible for supporting the coordination of studies, from protocol to final report (according to regulatory guidances)

Key Accountabilities

• Support / assist the Study Directors in the overall performance of studies
• Make sure that the administration is performed according to regulatory guidelines
• Make sure that the work performed will be described in the analytical report according to regulatory procedures
• Transfer all documentation relating to the research to the archivist for inclusion in the archive
• Learn how to ensure customer satisfaction in the long term and to answer questions
• Learn how to expand the relationship with the customer commercially so any follow-up assignments are awarded to ECL

Education

• MBO degree in Healthcare / Life Sciences

Skills

• Eager to learn and strong customer focus
• Excellent communication and interpersonal skills
• Good at establishing and maintaining internal and external relationships
• Energetic and enthusiastic with a flexible and dynamic work ethic
• Excellent command of Dutch and English, spoken and written
• Solid knowledge of Microsoft Office (Word / Excel)

Are you the driven, proactive colleague we are looking for and would you like to join our team? We would like to receive your CV including motivation via the application button.