Job Description
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.
Top Requirements:
- BS degree minimum
- 5-15 years of Medical Writing experience within the Medical Device industry
- 5+ years of recent experience independently authoring CERs, CEPs, PMCF Plans and Reports, and SSCPs
- Extensive editing and proofreading skills
- Strong communication skills to be affective while working remotely in support of cross-functional teams
- Ability to adapt to the client company's processes quickly
- Must have a proactive and collaborative mindset
- Readily available within normal working hours