Remote Medical Writer Consultant

Overview

A leading global manufacturer of cardiovascular medical devices is seeking a skilled

Medical Writer Consultant

to join their team until March 31, 2026. This is a full-time position requiring 40 hours per week. While the Manager and most of the Medical Writing team are based on the East Coast, we welcome applicants from anywhere in the U.S. as long as you are available during normal working hours.

Responsibilities

In this role, you will play a crucial part in developing essential documents such as Clinical Evaluation Reports (CERs), Clinical Evaluation Plans (CEPs), Post Market Clinical Follow-up (PMCF) Plans and Reports, and contributing to the Summary of Safety and Clinical Performance (SSCP) due by the end of March 2026. To excel in this position, you must quickly adapt to the established processes of our company and maintain a proactive, collaborative approach to your work.

Key Requirements

Bachelor\'s degree or higher.

5-15 years of experience in Medical Writing within the Medical Device industry.

5+ years of recent experience independently authoring CERs, CEPs, PMCF Plans and Reports, and SSCPs.

Exceptional editing and proofreading skills.

Strong communication skills to effectively engage with cross-functional teams while working remotely.

Ability to quickly adapt to company processes.

A proactive and collaborative mindset.

Available during normal working hours.

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