Clinical data Spec- Coordinator

FTPOL Fortrea Poland Sp z o.o.

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San Jose Until 8/21/2026 1+ years exp First posted June 6, 2026 Last posted June 6, 2026
Job description

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.

About this role

Summary

Support data acquisition, review, and quality checks for clinical trials in a collaborative environment.

Job title

Clinical Data Specialist – Coordinator

Experience level

1+ year

Minimum experience

1+ years exp

Industry

healthcare

Location requirements

Candidates must be based in Costa Rica, remote work not specified.

Salary

Not specified

Management role

No

Skills & keywords

Required skills

life sciencesclinical researchICH-GCPCDISCSDTMADaMproblem-solvingcommunicationMicrosoft Office

Preferred skills

None specified

Specializations

clinical datadata qualityclinical trials
Locations

Structured locations inferred from the posting.

Costa Rica

Remote Country