Clinical Data Management 📍 Location: Costa Rica (Costa Rica–based candidates only)
We are shaping the future of medicine through science, data, and collaboration. We are looking for a Sr Clinical Data Specialist based in Costa Rica to join our Clinical Data Management (CDM) team and play a key role in delivering high‑quality clinical trial data across a global portfolio.
About the role
In this role, you will be the subject‑matter expert for local laboratory data, ensuring accurate, timely, and compliant lab data delivery across clinical studies. You’ll work closely with internal teams, CROs, and vendors, contributing to study success from startup through database lock.
This is an excellent opportunity for a data management professional located in Costa Rica who enjoys cross‑functional collaboration, vendor oversight, and continuous process improvement.
What you’ll do
Lead and oversee local lab data activities for in‑house and outsourced clinical studies
Partner with CROs, vendors, and clinical sites to ensure high‑quality lab data collection, transfer, reconciliation, and query resolution
Support study startup, maintenance, and database lock activities related to local labs
Maintain and manage local lab analytes, LNR entries, and lab data standards
Represent Local Labs Data Management in project team meetings as a subject matter expert
Collaborate with Clinical Operations, Biometrics, Medical, and Regulatory teams
Identify opportunities to improve processes, automation, and data quality
Ensure compliance with ICH‑GCP, FDA regulations, and internal standards
What you bring
Bachelor’s degree (health sciences, life sciences, technology, or related field) or equivalent experience
3+ years of experience in Clinical Data Management or drug development
Strong knowledge of local lab data management best practices and technologies
Experience working with CROs and external vendors
Solid understanding of clinical trial documents and processes
