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Working as a CPM you will have to co-ordinate efforts of cross-functional project teams to support milestone achievement and to manage study issues and obstacles. You will ensure compliance with standard processes, policies and procedures. You will work together with the team in order to develop study management plans and serve as primary project contact with Sponsor.Profile:Bachelor's degree in life sciences or related field and 5 years’ clinical research experience including 2 years’ project management experience.Depth knowledge of and skill in applying applicable clinical research regulatory requirements.Competencies:Working as a team will be essential. You should have strong communication and interpersonal skills and excellent customer services skills.You need to be successful at solving problems and have demonstrated ability to deliver results to the appropriate quality and timeline metrics.The right CPM must have good therapeutic and protocol knowledge.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.