Clinical Data Manager, Third-Party Data Acquisition (Sponsor-Dedicated)

📍 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.

• →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, and inspections
• →Support and informally train coordinators and peers on study and vendor‑specific considerations
• →Contribute to process improvements and data integration optimization initiatives

• 3–5 years of 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

• BS/BA required, preferably in Life Sciences, Health, Technology, or equivalent experience

✅ This position requires candidates to be based in Costa Rica