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Clario
Clario
5,001 – 10,000 Employees
H1B Visa SponsorConsultingHealthcareLogistics
Clario develops technology and services that support clinical trials from study initiation through implementation. Its clinical trial management platform brings together solutions for electronic clinical outcome assessments, cardiac safety, medical imaging, precision motion, and respiratory monitoring across therapeutic areas such as oncology, cardiology, and neurology. Clario also applies artificial intelligence to endpoint analysis, helping research teams collect consistent trial data while supporting patient privacy and safety. The company works with decentralized and hybrid study models and serves clinical research programs across a global network of countries. Careers at Clario offer opportunities to contribute to healthcare technology, clinical data operations, and the development of tools used in drug research.
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Data Coordinator I (Remote in Costa Rica)

Clario is hiring a Data Coordinator I in Costa Rica to support clinical trial data quality. The role focuses on investigating discrepancies, processing corrections, and maintaining study records.

CRCosta RicaRemoteFull-timeJuniorNo degree requiredEnglish RequiredData CoordinatorGeneral

Description

  • Investigate data correction requests and discrepancies using established SOPs and work instructions
  • Accurately process source data, resolutions, and revisions across operational systems
  • Organize assigned work, prioritize requests, and support turnaround and departmental performance targets
  • Keep study documentation accurate and complete throughout the study lifecycle
  • File source documents and archive completed studies
  • Assist with data reconciliation and complete database updates within sponsor-defined timelines
  • Work with global Data Coordination and Data Management teams
  • Attend meetings related to assigned studies
  • Share observations about data quality and emerging trends

Requirements

  • A bachelor’s degree in life sciences or a related discipline is preferred, or at least one year of relevant experience
  • Careful and detail-oriented approach to identifying and investigating discrepancies
  • Strong ability to organize tasks and set priorities
  • Clear written and spoken communication skills
  • Ability to work effectively with colleagues across international teams
  • Comfortable using Microsoft Word, Excel, Outlook, and other computer systems
  • Accurate data-entry and typing abilities
  • Proactive attitude toward learning and solving problems
  • Ability to transfer prior knowledge to unfamiliar situations and work with growing independence
  • Commitment to continuous improvement
  • Willingness to recognize opportunities to improve processes and work practices

Benefits

  • Competitive compensation
  • Remote work arrangement available within Costa Rica
  • Structured practical training to support professional development
  • Experience working with global teams, sponsors, and diverse clinical studies
  • Pathways to build capabilities and advance in Clinical Data Management
  • Inclusive workplace committed to equal opportunity

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