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Associate English Costa Rica Jobs (NOW HIRING)

FreeBalance

Project Manager (Costa Rica)

Houston, TX · On-site

English and Spanish language fluency mandatory Qualifications: * Degree in University Information ... Knowledge of HRM/Payroll System in the public sector, particularly in Costa Rica, is an asset.

FreeBalance

Project Director (Costa Rica)

Miami, FL · On-site

English and Spanish language fluency mandatory Qualifications: * Degree in University Information ... Knowledge of HRM/Payroll System in the public sector, particularly in Costa Rica, is an asset.

FreeBalance

Project Director (Costa Rica)

Miami, FL

English and Spanish language fluency mandatory Qualifications: * Degree in University Information ... Knowledge of HRM/Payroll System in the public sector, particularly in Costa Rica, is an asset.

FreeBalance

Project Director (Costa Rica)

Miami, FL

English and Spanish language fluency mandatory Qualifications: * Degree in University Information ... Knowledge of HRM/Payroll System in the public sector, particularly in Costa Rica, is an asset.

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Associate Clinical Data Manager -Costa Rica (Home Based)

Fortrea

San Jose, CA • On-site, Remote

Full-time

Posted 7 days ago

Fortrea rating

7.2

Company rating: 7.2 out of 10

Based on 9 frontline employees who took The Breakroom Quiz

45th of 57 rated research

Job description

Associate Clinical Data Manager (ACDM)

📍 Based in Costa Rica (Mandatory)
🌎 Global Clinical Research Environment

Are you passionate about clinical data quality and global collaboration? We're looking for an Associate Clinical Data Manager (ACDM) based in Costa Rica to support the acquisition, quality, and compliance of external clinical trial data across multiple studies.

What you'll do
  • Support the endtoend acquisition of thirdparty (nonEDC) clinical data for assigned studies
  • Ensure data integrity, quality, compliance, and audit readiness throughout the data lifecycle
  • Collaborate with external vendors to align on timelines, processes, and issue resolution
  • Partner with crossfunctional study teams to support study objectives
  • Monitor data deliverables and proactively identify and resolve risks or inconsistencies
  • Represent ACDM activities in study team meetings, audits, and inspections
  • Support and informally train coordinators and peers on study and vendorspecific considerations
  • Contribute to process improvements and data integration optimization initiatives
What you bring
  • 3-5 years of experience in Clinical Data Management and/or drug development
  • Experience supporting thirdparty clinical data acquisition and vendor oversight
  • Solid understanding of:
    • Clinical trial processes, ICHGCP, and global regulatory requirements
    • Clinical data standards (CDISC, SDTM, ADaM) and data governance practices
    • NonEDC data sources and data integration processes
  • Strong organizational, problemsolving, and project coordination skills
  • Effective communication and collaboration across functional teams
  • High attention to detail and commitment to quality and compliance
Education
  • BS/BA required, preferably in Life Sciences, Health, Technology, or equivalent experience
Important

This position requires candidates to be based in Costa Rica

Why join us
  • Exposure to multiple therapeutic areas and development phases
  • Collaboration with global teams and innovative data technologies
  • Opportunity to make a meaningful impact on clinical development programs

Learn more about our EEO & Accommodations request here.

Apply