Regulatory Affairs Writer

4 days ago


Durham, North Carolina, United States Lifelancer Full time
Your Role and Responsibilities

As a Medical Writer II, you will be responsible for researching, creating, editing, and coordinating the production of clinical documents. This includes study protocols, model informed consents, interim and final clinical study reports, and safety update reports. You may also serve as the primary client contact.

You will need to demonstrate attention to detail, proactivity, and the ability to efficiently manage time spent on tasks. Prioritizing workload with attention to detail and organizational skills are crucial. Additionally, you will need to negotiate on behalf of medical writing to ensure resources, timelines, and expectations are aligned.



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