Clinical Data Specialist - Costa Rica (Home Based)

Join our Clinical Data Management team as a Clinical Data Specialist to ensure high-quality local laboratory data supporting global clinical trials. Collaborate with cross-functional teams and external partners from study start-up through database lock.

Location: Costa Rica (candidates must be currently based in Costa Rica)

Responsibilities

• Support local laboratory data activities for clinical studies (in‑house and outsourced), ensuring timely and high‑quality 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

Requirements

• 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 fast‑paced, global environment
• Bachelor’s degree in life sciences, health‑related, or technology‑related field (or equivalent experience)