Clinical Data Specialist – Remote (Costa Rica)

About the role

We are looking for a Clinical Data Specialist to join our Clinical Data Management team in Costa Rica. You will ensure high‑quality laboratory data for global clinical trials, collaborating with cross‑functional teams and external partners.

Key responsibilities

• Support local laboratory data activities for clinical studies (in‑house and outsourced), delivering timely, high‑quality results.
• 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.
• 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.
• Drive continuous‑improvement initiatives, including process optimisation, automation, and adoption of new technologies.

Required profile

• 2+ years of experience in Clinical Data Management or drug development.
• Strong knowledge of local laboratory data management within clinical trials.
• Familiarity with ICH/GCP and relevant regulatory standards.
• 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).

Required skills

• Veeva Vault (Local Lab Module)

What we offer

• Direct impact on data integrity and trial success.
• Collaborative global environment.
• Opportunities to develop expertise in a high‑demand area of clinical research.