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 when needed
- Work across multiple studies with diverse data sources and therapeutic areas
What You Bring
- 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
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. 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.
Skills Required
- 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
What We Do
Fortrea (Nasdaq: FTRE) is a leading global provider of clinical development and patient access solutions to the life sciences industry. We partner with emerging and large biopharmaceutical, medical device and diagnostic companies to drive healthcare innovation that accelerates life changing therapies to patients in need. Fortrea provides phase I-IV clinical trial management, clinical pharmacology, differentiated technology-enabled trial solutions and post-approval services. Fortrea’s solutions leverage three decades of experience spanning more than 20 therapeutic areas, a passion for scientific rigor, exceptional insights and a strong investigator site network. Our talented and diverse team working in more than 90 countries is scaled to deliver focused and agile solutions to customers globally. Learn more about how Fortrea is becoming a transformative force from pipeline to patient at Fortrea.com.
