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Должностные инструкции


As a Clinical Research Associated you are at the spot where science meets practice and New Health becomes alive! By establishing strong relationships to the involved investigators and the support functions on site like nurses, pharmacists etc. you become a real partner in the Phase II / III trials. Monitoring the progress of a trial by ensuring that ethical, legal and scientific standards, expressed in ICH/GCP (Good Clinical Practice)

In general as a CRA you might cover different trials and sites in different spots of your country. After you have been trained and gathered some experience at Quintiles, in many cases an option to work also home based is given. Independent whether working from home or the office, you will be fully integrated in a global working team and get in touch with peers from all over the world.

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Clinical Trials Assistant

As a Clinical Trials Assistant, you will have the opportunity to enter in the clinical research area, receive all trainings that support the function and know the protocols of the studies.

Moreover, you will be in contact with the CRAs, project managers and will also interact with the regulatory area, which will give you an accurate view of all areas of the company, and will help you to define the direction that you will give to your career.

The Clinical Trials Assistant (CTA), may act as a central contact for the clinical team for designated project communications, correspondence and associated documentation. Perform administrative tasks to support team members with clinical trial execution as needed and will also support the clinical project team in the several areas.

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