Clinical data Spec- Coordinator
San Jose
- Pay
- Pay not listed
- Work setting
- Not stated
- Employment
Full-time — employment source
Employment type in the employer’s posting: Full time
From the employer’s posting
Before you apply
- Eligibility
📍 Location: Costa Rica (candidates must be based in Costa Rica) 🧬 Department: Clinical Data Management — eligibility source
📍 Location: Costa Rica (candidates must be based in Costa Rica) 🧬 Department: Clinical Data Management
Read the full posting
What you’ll work on
Full postingSupport acquisition, review, and integration of external clinical trial data
Coordinate with internal teams and external vendors on accurate, timely data delivery
Perform data quality checks and help resolve discrepancies
Contribute to study deliverables under experienced data leads
Help prioritize tasks, manage timelines, and escalate issues
From the employer’s posting
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
Help prioritize tasks, manage timelines, and escalate issues when needed
What you’ll bring
All qualificationsCore experience
- Bachelor's degree in Life Sciences, Health Sciences, Technology, or related field (or equivalent experience)
- Basic understanding of clinical trials, ICH-GCP, and data quality principles
- Strong attention to detail and problem-solving skills
- Proficiency in Microsoft Office tools
Qualification wording
Bachelor’s degree in Life Sciences, Health Sciences, Technology, or related field (or equivalent experience)
Basic understanding of clinical trials, ICH-GCP, and data quality principles
Strong attention to detail and problem-solving skills
Proficiency in Microsoft Office tools
Education & alternatives
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
Posting record
Report an errorOpen 4 monthsWe first saw this posting 145 days ago and it is still up. Roles open this long are often slow to fill or kept open to collect applications.
- Status in our records
- Live
- First seen by us
- Jun 6, 2026 · 145 days ago
- Recorded sightings
- 312
- Last seen by us
- Oct 30, 2026
These dates show when we found the posting. Check the employer’s website to confirm it is still accepting applications.
Your next step
- Have your resume and examples of relevant work ready.
- Check the listed location, eligibility and core experience before starting.
- Ask the employer about the pay range before committing time to the process.
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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.
Source details
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- Pay
No pay amount identified in the saved description.
- Location & working pattern
San Jose
Clinical Data Specialist – Coordinator 📍 Location: Costa Rica (candidates must be based in Costa Rica) 🧬 Department: Clinical Data Management Advance clinical research through data precision
- Work authorization
No clear work-authorization passage found. Eligibility is unconfirmed.
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