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The Clinical Operations Summer Intern is responsible for providing daily support to the Clinical Trial Associates and Clinical Trial Managers in all aspects of clinical trial activities. They will perform routine duties associated with document management and submission to the Trial Master File, as well as assisting with the activities of the study team. The Clinical Operations intern works under direct supervision on tasks that require minimal discretion.
Job Responsibility:
Route documentation for appropriate signage
Assist with ordering materials needed for clinical studies
Update enrollment status for assigned trials and help to develop and maintain tracking tools
Coordinate project meetings, prepare agendas, and take minutes
Perform other duties as assigned
Requirements:
Enthusiasm to learn
Possesses sound communication skills, sufficient to clearly understand detailed instructions
Exhibits reliable ability to independently prepare and process routine documentation
Basic computer skills to support operation of clinical trial databases and electronic filing methods
Bachelor’s degree candidates who have completed 2+ years and are pursuing a degree in life sciences