IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com
IQVIA is a world leader in using data, technology, advanced analytics, and expertise to help customers drive healthcare - and human health - forward. Together with the companies we serve, we are enabling a more modern, more effective and more efficient healthcare system, and creating breakthrough solutions that transform business and patient outcomes.
To get there, it takes diverse skills and a curiosity to explore new possibilities. No matter your role, everyone at IQVIA contributes to our shared goal of improving human health. Thank you for your interest in growing your career with us.
Ihre Aufgaben
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Performing site selection, initiation, monitoring and close-out visits
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Supporting the development of a subject recruitment plan
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Evaluating the quality and integrity of site practices in accordance with regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
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Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution
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Collaborating with experts at study sites and with client representatives
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Depending on client model there might be remote-monitoring, involvement in study start-up processes, specialization on therapeutic area (pharmaceutical product or medical devices),
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Resources that promote your career growth
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Leaders that support flexible work schedules
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Programs to help you build your therapeutic knowledge
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Dynamic work environments that expose you to new experiences
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Home-office, company car, accident insurance and more
Whatever your career goals, we are here to ensure you get there!
Ihr Profil
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University Degree in life science or other scientific discipline or apprenticeship in the health care field
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Minimum of one year of on-site monitoring experience
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Knowledge of applicable clinical research regulatory requirements i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
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Strong written and verbal communication skills, attention to detail and ability to work in a fast pace environment
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Fluency in German on at least C1 level and a good command of English
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Flexibility to travel up to 40-60% of working time
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Driver's license class B