Medical Writer in Costello Medical's Medical Communications team specializing in scientific publications and communication of clinical trial data. Collaborating with clients to deliver high - quality scientific materials.
AB
Hybrid Medical Writer II – Clinical Evaluation Reporting, Medical Devices
Posted 3 months ago
About the role
- 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
Job type
Experience level
Salary
Degree requirement
Location requirements
RN specializing in clinical documentation integrity for pediatric patients at Connecticut Children's. Collaborating with healthcare providers to enhance documentation standards and accuracy.
Principal Medical Writer at IQVIA producing inspection - ready Clinical Study Reports for Phase 1 studies. Collaborating with teams to ensure compliance with regulatory and internal guidelines while maintaining document quality.
Principal Digital Medical Writer translating complex scientific evidence into engaging medical communications. Leading evidence synthesis projects and collaborating with digital, data, and design teams in a hybrid role.
Medical Writer creating and reviewing regulatory and public - facing documents. Supporting clinical and regulatory strategies with an emphasis on compliance and health literacy principles.
Senior Medical Writer overseeing high - quality clinical and regulatory documents at Ipsen, a biopharmaceutical company. Leading cross - functional teams and contributing to regulatory strategy while ensuring compliance and innovation in medical writing practices.
Medical Writer I role focusing on document management within Veeva systems for clinical projects. Supporting compliance and adherence to GxP guidelines while collaborating with stakeholders.
Medical Copywriter creating pharmaceutical promotional content for a global digital agency. Developing strategies and overseeing editorial quality for marketing communications in the life sciences sector.
CDI Nurse assisting GBMC Health Partners with documentation improvement efforts. Collaborating with physicians and clinicians on patient records and risk management.
Clinical Documentation Specialist working with healthcare teams to ensure accurate medical record documentation. Aiding in compliance and coding education for clinical documentation improvement.