Medtronic Clinical Studies Specialist CSHDM in Maastricht, Netherlands
Clinical Studies Specialist CSHDM
Maastricht, Limburg, Netherlands
Jul 13, 2017
Clinical Studies Specialist CSHDM - Coronary and Structural Heart Disease Management
For our Bakken Research Center in Maastricht, the Netherlands.
A Day in the Life
In this role you will perform a wide variety of tasks, directly supporting our clinical study managers. You will part of a world-wide project team working on coronary studies. . You will contribute to planning and implementation of clinical studies in line with local regulatory requirements. You will be support ethical committee submissions and ensure that all required filing and reporting has been done according to the clinical investigation plan. You will manage, track and document study product orders and ensure timely delivery and return. You facilitate and attend meetings (e.g. study team, vendors, investigators) and organize travel and documentation. Next to this you will prepare and distribute study documentation and communications both internal and external. Within this role you liaise with other departments (e.g. legal, contracts payments) to facilitate the creation of study agreements and execute payments. Flawless data entry, data processing and data reviews are an important part of your job. In this role you will also collect required documents to ensure timely availability.
• Bachelor or Masters degree in Life Sciences
• 2-3 years administrative experience
• Experience within a clinical study / research environment or safety reporting
• Knowledge of medical terminology
• Good knowledge of MS Office
• Fluency in English
We are looking for a customer focused team player with a distinct eye for detail. To be successful in this role you need to be result, as well as quality oriented. Your strong organizational skills enable you to manage multiple tasks at the same time. As part of a large international clinical team, some interpersonal and communication talent will make your job easier.
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