Regulatory Writing Intern - Medical Devices

November 4

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Description

β€’ The Regulatory Writing Intern participates in daily training and completes a 12-month program to become proficient in CER writing tasks. β€’ Initially, complete only non-billable training assignments, transition to billable assignments supporting current projects.

Requirements

β€’ Minimum of an MA or MS in science, engineering, technical writing or medical field; doctorate degree strongly preferred. β€’ Entry-level position (0-2 years medical writing/industry experience). β€’ Strong command of medical and surgical terminology. β€’ Oral and written fluency in English is required. β€’ Must be a U.S. resident

Benefits

β€’ Full-time, hourly employee with benefits.

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