Clinical Data Specialist- Costa Rica (Home Based)

 Posted 3 hours ago
     
⭐ 2-5 years experience
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AI Summary

The role involves managing local laboratory data for clinical trials to ensure accuracy, compliance, and high-quality deliverables. Responsibilities include configuring analyte parameters in Veeva Vault and collaborating with cross-functional teams from study start-up to database lock.

🚀 We’re hiring: Clinical Data Specialist – Clinical Data Management (Costa Rica)
📍 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 high‑quality local laboratory data that supports the success of global clinical trials. You’ll collaborate with cross‑functional teams and external partners (labs/CROs), helping drive accuracy, compliance, and operational excellence from study start‑up through database lock.

What you’ll do

  • 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

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

✨ Why this role You’ll have direct impact on data integrity and trial success, work in a collaborative global environment, and further develop your expertise in a high‑demand area of clinical research.

✅ 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.

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