Fortrea
Clinical data Spec- Coordinator
San Jose
Sponsorship not specifiedDetected 16 days ago
GCPClinical TrialsClinical ResearchResearchCommunicationCollaborationProblem SolvingMicrosoft Office
About the role
- 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.
Responsibilities
- Support the acquisition, review, and integration of external clinical trial data throughout the study lifecycle
- Perform data quality checks and assist in resolving discrepancies
- Contribute to study deliverables under the guidance of experienced data leads
- Help prioritize tasks, manage timelines, and escalate issues when needed
- 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.
- Ability to manage multiple priorities in a dynamic environment
- 📚 Build expertise in clinical data and external data integration
- 🤝 Collaborate with cross-functional and international teams
Requirements
- Approximately 1+ year of experience in clinical research or drug development
- Familiarity or interest in clinical data standards (e.g., CDISC, SDTM, ADaM)
- Proficiency in Microsoft Office tools
- ✅ Candidates must be currently based in Costa Rica
- Costa Rica (candidates must be based in Costa Rica)
Benefits
- Bachelor's degree in Life Sciences, Health Sciences, Technology, or related field (or equivalent experience)
Company info
- We are looking for a detail-oriented and collaborative Clinical Data Specialist - Coordinator to join our growing Clinical Data Management team.
Apply directly at Fortrea →Create a free account for alerts like thisView Fortrea immigration profile
This listing is sourced directly from Fortrea's careers page and normalized into a canonical job model.