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An established industry player is seeking a dedicated professional to coordinate clinical studies globally. This role involves providing crucial support to principal investigators and their teams through on-site training and monitoring of clinical data. You will ensure compliance with Good Clinical Practice (GCP) and regulatory standards while managing study-related administration and logistics tasks. Join a reputable organization with a rich history in developing specialized medical products, where your contributions will directly impact the quality and success of clinical research.
Coordinate clinical studies execution in clinical sites worldwide.
Provide support to principal investigators and their team: on-site trainings, monitoring of sites and clinical data, manage study-related administration and logistics tasks.
Ensure that studies and data management are performed in compliance with GCP, Ethical and Regulatory frame.
Werfen, founded in 1966, is a worldwide developer, manufacturer, and distributor of specialized medical products.