Clinical Data Specialist- Costa Rica (Home Based)
đ Weâre hiring: Clinical Data Specialist â Clinical Data Management (Costa Rica)
đ Location: Costa Rica (candidates must be currently based in Costa Rica)
Do you enjoy turning complex lab data into clean, reliable clinical insights? Join our Clinical Data Management team as a Clinical Data Specialist and play a key role in ensuring highâquality local laboratory data that supports the success of global clinical trials. Youâll collaborate with crossâfunctional teams and external partners (labs/CROs), helping drive accuracy, compliance, and operational excellence from study startâup through database lock.
What youâll do
Support local laboratory data activities for clinical studies (inâhouse and outsourced), ensuring timely and highâquality deliverables
Review study protocols and local lab requirements to identify required analytes
Maintain and support a Global Analyte Library, aligned with internal laboratory standards
Partner with Clinical Operations, Biometrics, Medical Monitoring, and Regulatory teams to align lab data with study timelines and milestones
Proactively identify risks and issues related to lab data collection, transfer, and quality, and support mitigation plans
Configure laboratory locations and analyte parameters in systems such as Veeva Vault Local Lab Module
Champion continuous improvement initiatives, including process optimization, automation, and adoption of new technologies
What youâll bring
2+ years of experience in Clinical Data Management and/or the drug development process
Strong knowledge of local laboratory data management within clinical trials
Familiarity with ICH/GCP and regulatory standards applicable to clinical data
Ability to manage multiple studies or priorities in a fastâpaced, global environment
Bachelorâs degree in life sciences, healthârelated, or technologyârelated field (or equivalent experience)
⨠Why this role Youâll have direct impact on data integrity and trial success, work in a collaborative global environment, and further develop your expertise in a highâdemand area of clinical research.
â Important: This role is based in Costa Rica, and we can only consider candidates currently located in Costa Rica.
Learn more about our EEO & Accommodations request here.
đ Location: Costa Rica (candidates must be currently based in Costa Rica)
Do you enjoy turning complex lab data into clean, reliable clinical insights? Join our Clinical Data Management team as a Clinical Data Specialist and play a key role in ensuring highâquality local laboratory data that supports the success of global clinical trials. Youâll collaborate with crossâfunctional teams and external partners (labs/CROs), helping drive accuracy, compliance, and operational excellence from study startâup through database lock.
What youâll do
Support local laboratory data activities for clinical studies (inâhouse and outsourced), ensuring timely and highâquality deliverables
Review study protocols and local lab requirements to identify required analytes
Maintain and support a Global Analyte Library, aligned with internal laboratory standards
Partner with Clinical Operations, Biometrics, Medical Monitoring, and Regulatory teams to align lab data with study timelines and milestones
Proactively identify risks and issues related to lab data collection, transfer, and quality, and support mitigation plans
Configure laboratory locations and analyte parameters in systems such as Veeva Vault Local Lab Module
Champion continuous improvement initiatives, including process optimization, automation, and adoption of new technologies
What youâll bring
2+ years of experience in Clinical Data Management and/or the drug development process
Strong knowledge of local laboratory data management within clinical trials
Familiarity with ICH/GCP and regulatory standards applicable to clinical data
Ability to manage multiple studies or priorities in a fastâpaced, global environment
Bachelorâs degree in life sciences, healthârelated, or technologyârelated field (or equivalent experience)
⨠Why this role Youâll have direct impact on data integrity and trial success, work in a collaborative global environment, and further develop your expertise in a highâdemand area of clinical research.
â Important: This role is based in Costa Rica, and we can only consider candidates currently located in Costa Rica.
Learn more about our EEO & Accommodations request here.