Medical Writer II providing strategic writing expertise for Clinical Evaluation Reporting documents at Abbott. Collaborating on clinical evaluation projects for medical devices across multiple sites.
Responsibilities
Writes and contributes to Clinical Evaluation reporting deliverables including Clinical Evaluation Plans/Reports, SSCPs, Regulatory Responses
Evaluates and summarizes clinical evidence from clinical investigations, literature, post-market surveillance
Analyzes results in preparation for product applications and submissions
Collaborates with team members and stakeholders for CER related projects
Supports additional clinical, regulatory, quality and engineering related deliverable as assigned
Communicates and collaborates with Regulatory Affairs, Marketing, Quality Engineering, Clinical Affairs, Risk Management and Medical Affairs
Requirements
Bachelor's degree in Science, Medical Technology, English OR 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
Must possess comprehensive written and verbal communication skills
Multitasking, prioritization and meeting deadlines in a timely manner
Strong organizational and follow-up skills
Ability to critically review own work
Strong verbal and written communication skills
Benefits
Career development with an international company
Free medical coverage in the Health Investment Plan (HIP) PPO medical plan
Excellent retirement savings plan with high employer contribution
Tuition reimbursement
Freedom 2 Save student debt program
FreeU education benefit - an affordable and convenient path to getting a bachelor’s degree
Recognized as a great place to work in dozens of countries
Recognized as one of the best big companies to work for
Job title
Medical Writer II – Clinical Evaluation Reporting, Medical Devices
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