You will be part of a young and dynamic multi-disciplinary project research team. Part of your responsibilities will be to perform clinical monitoring of designated projects in accordance with applicable SOPs and regulations. This will involve travelling to clinical sites located mainly in Europe to perform source data verification in addition to other specific, site-related activities. The remainder of the time will be office-based and will be spent, amongst others, performing tasks in data management such as checking clinical data for completeness and medical consistency, in preparation for statistical analysis.

Skills

ü             Strong regulatory knowledge including ICH GCP, ISO guidelines...

ü             Excellent interpersonal, verbal and written communication skills.

ü             Sound problem solving skills.

ü             Client focussed approach to work, ability to interact professionally within a client organisation.

ü             Ability to prioritize multiple tasks and achieve project timelines.

ü             Able to travel a minimum of 35% (average); be in possession of a valid driving licence.

ü             Show commitment to and perform consistently high quality work; eye for detail.

ü             Strong computer and internet skills including knowledge of MS-Office products.

Education

Educated to degree level (biological science, nurse, pharmacy or other health related discipline) or other equivalent experience.

Languages

Be fluent in English (oral and written) with good knowledge of German and at least one other European language.