A leading global manufacturer of cardiovascular medical devices is in immediate need of a remote Medical Writer consultant to support them until 3/31/2026. This is a 40 hours/week position. The Manager, along with most of the Medical Writing team, is based on the East Coast but this consultant can be based anywhere in the US as long as you can be readily available during normal working hours.
The Medical Writer will be responsible for the independent and hands-on development of Clinical Evaluation Reports (CERs), the Clinical Evaluation Plan (CEP), the Post Market Clinical Follow-up (PMCF) Plan and Report, and will support the Summary of Safety and Clinical Performance (SSCP) that are due by 3/31/2026. This consultant needs to be able to quickly adapt to the company's process and have a proactive and collaborative approach to be successful in this role. This consultant will not be focused on changing or optimizing processes.
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