
Clinical Research Associate II
Posted May 9

Posted May 9
This is a fully remote position, open to applicants in Spain.
β’ Conducts on-site or remote Pre-Study, Initiation, Interim, and Close-Out monitoring visits to ensure that the facilities and personnel at the investigational site remain sufficient for the study's execution.
β’ Identifies investigators and confirms that they possess the necessary qualifications, resources, facilities, equipment, and staff to conduct the clinical study throughout its duration.
β’ Provides training to the staff of the investigational site as needed.
β’ Assists in the preparation of regulatory and/or Ethics Committee submissions when applicable.
β’ Bachelor's degree in Life Sciences or a comparable combination of education, training, and experience.
β’ Significant on-site monitoring experience in phase 2/3 clinical trials, preferably with a background in complex studies such as oncology or rare diseases.
β’ Proficient in English at a full working level.
β’ Capable of planning, multitasking, and thriving in a dynamic team environment.
β’ Strong communication, collaboration, and problem-solving abilities.
β’ Willingness to travel.
β’ Opportunities for internal training and career development.
β’ A strong focus on personal and professional advancement.
β’ A friendly and supportive work environment.
β’ The chance to collaborate with colleagues from around the globe, with English as the primary language of communication.
Worldwide Clinical Trials
Gartner
AccessLex Institute
ICON plc
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