Senior Medical Writer, Clinical Evaluation (on-site)

Our location in Maple Grove MN, St. Paul, MN, Plymouth, MN, Plano TX or Santa Clara, CA currently has an on-site opportunity for a Senior Medical Writer, Clinical Evaluation.  The Sr. Medical Writer on our Regulatory Clinical Evaluation team provides technical and strategic writing expertise throughout the product development and life cycle process. Daily activities are related to authoring Clinical Evaluation Reporting documents for the Neuromodulation, CAHF and Vascular products.  Experience in clinical study management and design, medical, or scientific writing, and/or quality engineering/risk management and strong written and verbal communication skills are needed. 

• Writes and contributes to Clinical Evaluation reporting deliverables including Clinical Evaluation Plans/Reports, PMS and PMCF Plans/Reports, SSCPs, Regulatory Responses and other related documentation. 
• Evaluates and summarizes clinical evidence including data from sources such as clinical investigations, literature, post-market surveillance, risk, and post market clinical evaluations.  Analyzes results in preparation for product applications and submissions.  
• Collaborates with team members and stakeholders in planning for and supporting CER related projects and processes.
• Supports additional clinical, regulatory, quality and engineering related deliverable as assigned.
• Effectively communicates and collaborates with Sales and Marketing, R&D, Regulatory Affairs, Library Services, Product Performance Group (PPG), Quality Engineering, Clinical Affairs, Clinical Science, Risk Management and Medical Affairs in completing clinical evaluation project related deliverables.
• Maintains thorough knowledge of assigned products. Identifies appropriate sources of relevant data, interprets, evaluates and incorporates information from various sources including literature, clinical data, and medical references.
• Reviews IFUs, patient guides, Risk Management files, Clinical Evaluation Protocols, Clinical Evaluation Reports and Plans (CER/CEP), physician training materials, ensuring alignment of risk information. Involved in responses to complex queries such as those issued by notified bodies and stakeholders.
• Authors and contributes to necessary documents for regulatory submissions and communications, risk reviews and other processes such as regulatory inquiries.
• Ensures quality in all deliverables and documentation with attention to detail, consistency and integrity of data.  Responsible for compliance with applicable corporate and divisional policies and procedures. Ensures compliance to applicable regulations and guidance’s (ISO13485, ISO14155, ISO14791, MEDDEV 2.7.1, MDR, and EU and FDA guidance documents) and applicable Abbott SOPs and DOPs.

• Bachelor’s degree in a Science, Medical Technology or equivalent technical degree OR an equivalent combination of education and work experience.
• Minimum 3 years’ relevant experience in a related area such as R&D, Technical Product Development, or Quality in a healthcare industry.
• Must possess comprehensive written and verbal communication, interpersonal, presentation, analytical, project management skills and the ability to prioritize and handle a large volume of projects simultaneously and meet deadlines.
• Writing, editing and managing engineering and technical documentation utilized in the development of new products and improvement of existing products.
• Developing spreadsheets or databases for the capture, assembly, and graphical presentation of metrics.
• Non-product application validation - Process establishment including metrics definition, statistical analysis and analytical techniques. 
• Experience in complaint handling, operation or service of diagnostic instrumentation, or medical technology.

In specific locations, the pay range may vary from the range posted.