Role Description The Senior Clinical Evaluation Medical Writer is responsible for authoring, reviewing, and managing clinical evaluation documents and reports in compliance with regulatory requirements and industry standards. This role involves synthesizing clinical data, scientific literature, and regulatory guidelines to create clear, concise, and evidence-based documentation that supports the safety and performance of medical devices. The writer collaborates closely with cross-functional teams to ensure the timely delivery of high-quality clinical evaluation reports (CERs) and related documents.

• Review and summarize scientific literature
• Appraise, analyze, summarize, and discuss clinical evidence from all available sources
• Conduct comprehensive literature searches and perform critical evaluations of clinical evidence
• Maintain a database of peer-reviewed literature
• Develop state of the art (SOTA) on product family for its intended purpose
• Create & maintain plans and reports for regulatory authorities, including but not limited to:
• Clinical Evaluation Plans (CEP)
• Clinical Evaluation Reports (CER)
• Post-Market Clinical Follow-up Plans (PMCF-P)
• Post-Market Clinical Follow-up Reports (PMCF-R)
• Summary of Safety and Clinical Performance (SSCP)
• Periodic Safety Update Reports (PSUR)
• Report instances of complaints/adverse events from literature
• Create responses for audit/submission queries

Qualifications

• Baccalaureate degree and minimum of 4 years relevant experience OR advanced degree with minimum of 2 years relevant experience

Requirements

• Knowledge of regulatory agencies’ guidelines on clinical evaluation requirements
• Experience writing clinical evaluation documents
• Medical Device experience
• Strong project management skills
• Strong communication skills
• Ability to deliver and manage projects assigned and work with other stakeholders to achieve desired results

Company Description