You coordinate the set-up and closure of databases used for data capture in clinical research projects. You work in a highly regulated and challenging environment. You are involved in maintaining quality of the developed products in accordance with all relevant SOPs and guidelines. You collaborate with third parties either in-house or external, and ensure that the databases are compliant to the clinical study protocol and that the overall objectives are met. You provide clear budget and status overview to both our customers and internally.
Profile: By preference, you have a master degree with experience in (clinical) project management and strong affinity with technology. You are a detailed and technical oriented professional with good negotiation, time management and people skills. Experience in clinical research and/or data management is a plus.
Fluent in Dutch and English, good communication skills both verbally and in writing