Job Summary
A company is looking for a Sr. Technical Writer to join their MedTech Surgery business.
Key Responsibilities
- Plan and write Clinical Evaluation Reports (CERs), Clinical Evaluation Plans (CEPs), and Summary of Safety and Clinical Performance Reports (SSCPs)
- Mentor junior writers and conduct technical reviews for document accuracy and compliance
- Lead daily activities to ensure timelines are met and participate in process improvement initiatives
Required Qualifications, Training, and Education
- BA, BS, or BSN is required; advanced degree is preferred
- Minimum of 4 years of related job experience is required
- Experience within the medical device industry and knowledge of global clinical evaluation regulatory requirements
- Proven knowledge in clinical research and quality regulatory compliance is preferred
- Experience in document creation and associated evidence generation is necessary
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