A global full-service CRO is seeking a Sr. Regulatory Affairs Specialist Consultant for a 12-month contract in Colombia. In this client-facing role, you will provide operational and administrative support to regulatory activities in the Medical Devices portfolio. Responsibilities include managing regulatory documentation for submissions, performing checks, and assisting with regulatory plans. The ideal candidate holds a relevant bachelor's degree and understands Colombian medical device regulations. This position is entry-level, suitable for those with internship experience.
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