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Cra Ii - Madrid, España - Ergomed
Descripción
Job Description Performs on-site or remote Pre-Study, Initiation, Interim, and Close-Out monitoring visit activities to ensure that facilities and staff at the investigational site continue to be adequate for the conduct of the studyIdentifies the investigators and verifies that the investigator has adequate qualifications, resources, facilities, equipment and staff to conducting the clinical study throughout the study period.
Trains investigational site staff as necessary.When applicable, supports preparation of regulatory and / or EC submissions.
Qualifications College/University degree in Life Sciences or an equivalent combination of education, training & experienceExtensive on-site monitoring experience in phase 2/3 trials, ideally with experience of complex trialsFull working proficiency in English and GermanAbility to plan, multitask and work in a dynamic team environmentCommunication, collaboration, and problem-solving skillsAbility to travelAdditional InformationWhy Ergomed We prioritize diversity, equity, and inclusion by creating an equal opportunities workplace and a human-centric environment where people of all cultural backgrounds, genders and ages can contribute and grow.
To succeed we must work together with a human first approach.Why? because our people are our greatest strength leading to our continued success on improving the lives of those around us.
We offer:
Training and career development opportunities internally Strong emphasis on personal and professional growth Friendly, supportive working environment Opportunity to work with colleagues based all over the world, with English as the company language
