Medical Information Specialist (Medtech)

TL;DR

Medical Information Specialist (Medtech): Responding to drug information inquiries and managing adverse event reporting for healthcare professionals and patients with an accent on clinical accuracy and regulatory compliance. Focus on delivering high-quality medical communications and maintaining rigorous safety standards during US-aligned working hours.

Location: Must be based in Poland, Ireland, the UK, Italy, Portugal, Germany, or Spain and legally eligible to work in the EU or UK.

Company

hirify.global provides next-generation commercialization services to the life sciences industry, supporting innovative therapies and patient care globally.

What you will do

• Triage and respond to drug information inquiries from healthcare professionals and patients.
• Identify and document adverse events and product quality issues in compliance with SOPs.
• Translate medical documents and responses between English and Spanish.
• Perform medical writing for custom inquiry responses and safety narratives.
• Coordinate with Quality Assurance and Regulatory Affairs departments regarding product complaints.
• Evaluate medical literature to develop accurate information for dissemination.

Requirements

• Degree in Life Sciences or Healthcare (Pharmacy, Biomedical Sciences, etc.).
• English: C1 level required.
• Spanish: Native or mother tongue fluency required.
• Must be legally eligible to work in the EU or UK.
• Availability to work US hours (9-hour shifts between 2pm and 2am CET).
• Strong clinical background and excellent verbal/written communication skills.

Culture & Benefits

• Global organization committed to a healthier world and inclusive culture.
• Opportunity to work in a diverse, patient-minded environment.
• Focus on professional development and talent growth.
• Remote-first role with home office flexibility.