Remote Clinical Research Writer – Medical Devices

Arthrex; United States; Remote; USD 90,000 - 130,000; Full time

Benefits offered by this job

Medical Insurance

Dental & Vision

401(k) Matching

Annual Bonus

Tuition Reimbursement

FSA

Paid Time Off

EAP

Job summary

Arthrex, Inc. is seeking a Clinical Research Medical Writer to lead writing from concept through publication, with a focus on clinical study protocols and related documents. The role supports PMCF protocols, interim reports, and final study reports across global clinical research projects.

The position is fully remote with periodic travel to the Naples, Florida headquarters as business needs require. Strong background in medical writing, regulatory standards (EU MDR, FDA 21 CFR 812), and

Qualifications

• Master’s degree required; PhD preferred.
• 4 years of clinical research experience.
• 2 years of medical device writing experience.
• Strong knowledge of orthopedic terminology.
• Experience writing study protocols and manuscripts.

Responsibilities

• Manage writing from study concept to final report and publication.
• Develop clinical study protocols and related documents; support protocol amendments.
• Draft interim and final study reports and PMCF documents.
• Coordinate with product management, statistics, regulatory affairs, and CROs.
• Ensure documents follow procedures, guidelines, and templates.

Skills

Scientific writing

Medical writing

Regulatory knowledge

Project management

Literature review

Education

Master's degree

PhD preferred

Tools

Microsoft Word

Microsoft Excel

Microsoft PowerPoint

Job description

Arthrex, Inc. is seeking a Clinical Research Medical Writer to lead writing from concept through publication, with a focus on clinical study protocols and related documents. The role supports PMCF protocols, interim reports, and final study reports across global clinical research projects.

The position is fully remote with periodic travel to the Naples, Florida headquarters as business needs require. Strong background in medical writing, regulatory standards (EU MDR, FDA 21 CFR 812), and