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
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Review and ensure the quality and consistency of medical coded data delivered by external vendors
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Provide oversight of outsourced coding activities, including dictionary and synonym reviews
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Support MedDRA and WHO Drug Dictionary upversioning across multiple studies
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Act as a subject matter expert for dictionary usage and coding quality
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Identify and escalate coding-related issues, proposing clear and practical solutions
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Ensure compliance with ICH/GCP, regulatory requirements, and industry best practices
What you bring
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Degree in Life Sciences, Health-related field, or equivalent experience
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Fluent English (written and spoken)
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5+ years of experience in medical coding using MedDRA and WHO Drug Dictionaries
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Experience in a CRO, pharmaceutical, or biotechnology environment
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Strong attention to detail, ability to manage priorities, and a collaborative mindset
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Experience with coding tools (e.g., Veeva, Medidata RAVE Coder) is a plus
Why join us
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Work on global, high‑impact clinical research studies
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Be recognized as a medical coding and dictionary expert
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Collaborate with experienced, international teams
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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.
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