Clinical data Spec- Coordinator

San Jose, United StatesOn-site

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Requirements

experience in clinical research or drug development Basic understanding of clinical trials, ICH-GCP, and data quality principles Familiarity or interest in clinical data standards (e.g., CDISC, SDTM, ADaM) Strong attention to detail and problem-solving skills Effective communication and collaboration abilities Ability to manage multiple priorities in a dynamic environment Proficiency in Microsoft Office tools Why Join Us?
🌍 Work on global clinical trials across diverse therapeutic areas 📚 Build expertise in clinical data and external data integration 🤝 Collaborate with cross-functional and international teams 🚀 Grow your career in a supportive and structured environment Important Requirement ✅ Candidates must be currently based in Costa Rica Who You Are You are detail-driven, proactive, and eager to build a career in Clinical Data Management.

Clinical Data Specialist – Coordinator 📍 Location: Costa Rica (candidates must be based in Costa Rica) 🧬 Department: Clinical Data Management Advance clinical research through data precision We are looking for a detail-oriented and collaborative Clinical Data Specialist – Coordinator to join our growing Clinical Data Management team.
In this role, you will support the integrity, quality, and timely delivery of clinical trial data from external sources, contributing directly to studies that improve patient outcomes worldwide.
What You’ll Do Support the acquisition, review, and integration of external clinical trial data throughout the study lifecycle Coordinate with internal teams and external vendors to ensure accurate and timely data delivery Perform data quality checks and assist in resolving discrepancies Contribute to study deliverables under the guidance of experienced data leads Participate in study-related activities, including meetings and task coordination Help prioritize tasks, manage timelines, and escalate issues
You thrive in a collaborative environment, enjoy solving problems, and are motivated by contributing to high-quality clinical research.
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