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Open nowPosted 93 days ago

Clinical data Spec- Coordinator

Fortrea49 open roles

Where
San Jose
Work mode
Remote
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Your applicationOpen nowClinical data Spec- CoordinatorFortrea · San Jose

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The clock on this job

Early applications get read.

8.1% of postings close within 7 days. Measured by our own scanner across the market. Fortrea postings stay open a median of 4 days.

Share of postings closed within
  1. 1.7%1 day
  2. 3.6%3 days
  3. 8.1%7 days
  4. 15.1%14 days
  5. 34.0%30 days
This job: posted 93 days ago

Fortrea median: 4 days open

The posting

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.

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