Medical Writer

TL;DR

Medical Writer: Developing high-quality clinical documentation to support research and regulatory success with an accent on clarity, consistency, and compliance. Focus on managing the document development lifecycle, reviewing study protocols, and ensuring alignment with regulatory standards.

Location: Must be based in Costa Rica (Remote)

Company

hirify.global, a part of Thermo Fisher Scientific, is committed to transforming clinical trials through technology and innovation to unlock better evidence for life-changing therapies.

What you will do

• Review study protocols and contracts for inclusion/exclusion criteria and imaging objectives.
• Develop, write, and finalize study documentation including Site Manuals and Quick Reference Guides.
• Review and update Standard Operating Procedures (SOPs) related to Medical Communications.
• Manage the document development lifecycle, including version control and template maintenance.
• Provide guidance to project teams to ensure timely delivery of approved documentation.
• Ensure all documentation meets quality, regulatory, and internal compliance standards.

Requirements

• Bachelor’s degree in Life or Physical Sciences.
• Must be based in Costa Rica.
• 3+ years of experience in pharmaceutical, clinical, or imaging research environments.
• Strong working knowledge of clinical trial terminology and documentation standards.
• Proficiency in medical, regulatory, and clinical writing.
• Excellent attention to detail and organizational skills.

Nice to have

• 2+ years of medical writing experience.

Culture & Benefits

• Competitive compensation package.
• Comprehensive health and wellness benefits.
• Flexible work arrangements.
• Paid time off and company holidays.
• Professional development opportunities and engaging employee programs.