Associate Clinical Data Manager -Costa Rica (Home Based)

San Jose, United StatesOn-site

Requirements

experience in Clinical Data Management and/or drug development
Experience supporting third‑party clinical data acquisition and vendor oversight Solid understanding of: Clinical trial processes, ICH‑GCP, and global regulatory
requirements Clinical data standards ( CDISC, SDTM, ADaM ) and data governance practices Non‑EDC data sources and data integration processes Strong organizational, problem‑solving, and project coordination skills Effective communication and collaboration across functional teams High attention to detail and commitment to quality and compliance Education BS/BA required , preferably in Life Sciences, Health, Technology, or equivalent
experience Important ✅ This position requires candidates to be based in Costa Rica Why join us Exposure to multiple therapeutic areas and development phases Collaboration with global teams and innovative data technologies Opportunity to make a meaningful impact on clinical development programs Learn more about our EEO & Accommodations request here .

Associate Clinical Data Manager (ACDM) 📍 Based in Costa Rica (Mandatory) 🌎 Global Clinical Research Environment Are you passionate about clinical data quality and global collaboration? We’re looking for an Associate Clinical Data Manager (ACDM) based in Costa Rica to support the acquisition, quality, and compliance of external clinical trial data across multiple studies.
What you’ll do Support the end‑to‑end acquisition of third‑party (non‑EDC) clinical data for assigned studies Ensure data integrity, quality, compliance, and audit readiness throughout the data lifecycle Collaborate with external vendors to align on timelines, processes, and issue resolution Partner with cross‑functional study teams to support study objectives Monitor data deliverables and proactively identify and resolve risks or inconsistencies Represent ACDM activities in study team meetings, audits,