Medical Writer creating Clinical Evaluation Reporting documents for medical devices across multiple locations in the US. Involves technical and strategic writing expertise throughout product development and life cycle process.
Responsibilities
Writes and contributes to Clinical Evaluation reporting deliverables
Evaluates and summarizes clinical evidence
Analyzes results in preparation for product applications and submissions
Collaborates with team members and stakeholders in planning for and supporting CER related projects
Effectively communicates and collaborates with various departments
Requirements
Bachelor's degree in Science, Medical Technology, English OR an equivalent combination of education and work experience
Minimum 2 years relevant professional experience in R&D, Technical Product Development, Quality, Regulatory Affairs, Clinical Research, or Medical Writing
Comprehensive written and verbal communication skills
Strong organizational skills and attention to detail
Ability to critically review own work before sending out for internal/external review
Multitasking and prioritizing skills
Benefits
Career development with an international company
Free medical coverage in Health Investment Plan (HIP) PPO medical plan
Excellent retirement savings plan with high employer contribution
Tuition reimbursement
Freedom 2 Save student debt program and FreeU education benefit
Job title
Medical Writer II – Clinical Evaluation Reporting, Medical Devices
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