Associate Medical Writer, In Vitro Diagnostic Regulation (IVDR) - Remote

Overview

The Associate Medical Writer will leverage their regulatory writing expertise to support the development and management of regulatory-compliant performance evaluation reports for healthcare companies.

In Short

• Full-Time position.
• Remote work opportunity.
• Experience in writing CERs and/or PERs required.
• Collaboration with project managers and writing team.
• Strong command of medical and laboratory terminology.
• Effective written and verbal communication skills.
• Ability to manage multiple projects and deadlines.
• Training in science, engineering, or medical fields.
• Proficient in document management tools like Word and Excel.
• Proactive and adaptable to shifting priorities.

Requirements

• Previous experience in regulatory writing.
• Knowledge of MEDDEV and EU regulations.
• Strong organizational skills.
• Ability to work in a team setting.
• Scientific/research background.
• Attention to detail and quality control.
• Effective problem-solving skills.
• Initiative and sound judgment in unfamiliar situations.
• Ability to maintain effective working relationships.
• Willingness to attend internal meetings as needed.

Benefits

• Opportunity to work with top industry clients.
• Support for career development in medical writing.
• Work in a dynamic and collaborative environment.
• Flexible work arrangements.
• Competitive compensation package.