Provide monitoring visits and site management, intense interaction and communication with investigators, logistic support to the medical team, quality control on data and processes with a primary focus on patient safety are your daily tasks.You will work across a range of studies and therapy areas. You will be responsible for site management from selection over start up and recruitment till study closure. You will ensure that recruitment targets are met by building strong relationships with site staff whilst ensuring that the trial is run to the standards requirements.Profile: You should have a degree in a sciences and previous experience in clinical research; Master in Clinical Trials will be appreciated and willingness to travel at a national level is required.Competencies: Successful candidate should be able to communicate efficiently on different levels, be assertive and can work on several projects at once with high flexibility, be detail oriented and have excellent time management and organizational skills.In addition to this, you need to have high level of English.What we have to offer: We put special emphasis in offering the best training opportunities and fostering personal development. Our culture is based in improving the well-being of our employees, both at professional and personal levels. We offer flexibility, recognition and rewards as well as an attractive salary.