Remote EUMDR Medical Writer — CERs & CEPs Expert

Kelly Science, Engineering, Technology & Telecom; United States; Remote; USD 80,000 - 100,000; Full time

Benefits offered by this job

Medical, Dental, Vision benefits

401K options

Paid time off including holidays

Job summary

A global medical device consulting firm is looking for a EUMDR Medical Writer for a remote, full-time engagement. Candidates should have a minimum of 5 years of medical or scientific writing experience, ideally within the medical device industry, with knowledge of EU MDR requirements. The position offers full benefits and focuses on clinical documentation, literature reviews, and compliance with regulatory guidelines. Strong written and oral communication skills are essential. This role is an excellent opportunity to contribute to significant medical projects.

Qualifications

• 5 years experience in medical writing; less than 4 years with advanced degree may be acceptable.
• 3-5 years in the medical device industry with expertise in CER document creation.
• Ability to quickly develop therapeutic expertise.

Responsibilities

• Prepares clinical research documents for medical device registrations.
• Communicates with project managers and regulatory associates.
• Assists in literature searches and summarizes clinical literature.

Skills

Strong oral communication

Project management

Prioritization skills

Excellent interpersonal skills

Microsoft Office Suite proficiency

Education

5 years of related job experience in medical or scientific writing

Advanced degree (M.S. or higher) may be acceptable

Tools

Distiller

Endnote

Microsoft Word

Job description

A global medical device consulting firm is looking for a EUMDR Medical Writer for a remote, full-time engagement. Candidates should have a minimum of 5 years of medical or scientific writing experience, ideally within the medical device industry, with knowledge of EU MDR requirements. The position offers full benefits and focuses on clinical documentation, literature reviews, and compliance with regulatory guidelines. Strong written and oral communication skills are essential. This role is an excellent opportunity to contribute to significant medical projects.