About this role
Senior Coding Specialist 📍 Costa Rica ✅ Candidates must be based in Costa Rica Are you passionate about medical coding quality and clinical data integrity? We’re looking for a Senior Coding Specialist based in Costa Rica to support high‑quality, compliant clinical trial data across global studies. What you’ll do
• Review and ensure the quality and consistency of medical coded data delivered by external vendors • Provide oversight of outsourced coding activities, including dictionary and synonym reviews • Support MedDRA and WHO Drug Dictionary upversioning across multiple studies • Act as a subject matter expert for dictionary usage and coding quality • Identify and escalate coding-related issues, proposing clear and practical solutions • Ensure compliance with ICH/GCP, regulatory requirements, and industry best practices What you bring
• Degree in Life Sciences, Health-related field, or equivalent experience • Fluent English (written and spoken) • 5+ years of experience in medical coding using MedDRA and WHO Drug Dictionaries • Experience in a CRO, pharmaceutical, or biotechnology environment • Strong attention to detail, ability to manage priorities, and a collaborative mindset • Experience with coding tools (e.g., Veeva, Medidata RAVE Coder) is a plus Why join us
• Work on global, high‑impact clinical research studies • Be recognized as a medical coding and dictionary expert • Collaborate with experienced, international teams • Grow your career in Clinical Data Management 👉 Important: This position is based in Costa Rica, and applications will only be considered from candidates currently located in Costa Rica.
Learn more about our EEO & Accommodations request here.