Clinical data Spec- Coordinator

📍 Location: Costa Rica (candidates must be based in Costa Rica)
🧬 Department: Clinical Data Management

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.

• →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 when needed
• →Work across multiple studies with diverse data sources and therapeutic areas

• Bachelor’s degree in Life Sciences, Health Sciences, Technology, or related field (or equivalent experience)
• Approximately 1+ year of 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

✅ Candidates must be currently based in Costa Rica
 

You are detail-driven, proactive, and eager to build a career in Clinical Data Management. You thrive in a collaborative environment, enjoy solving problems, and are motivated by contributing to high-quality clinical research.

Learn more about our EEO & Accommodations request here.