Associate Clinical Data Manager (ACDM) Mexico

Associate Clinical Data Manager (ACDM)

Based in Mexico (Mandatory)
Global Clinical Research Environment

Are you passionate about clinical data quality and global collaboration Were looking for an Associate Clinical Data Manager (ACDM) based in Mexico to support the acquisition quality and compliance of external clinical trial data across multiple studies.

What youll do

• Support the endtoend acquisition of thirdparty (nonEDC) 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 crossfunctional 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 vendorspecific considerations
• Contribute to process improvements and data integration optimization initiatives

What you bring

• 35 years of experience in Clinical Data Management and/or drug development
• Experience supporting thirdparty clinical data acquisition and vendor oversight
• Solid understanding of:
  • Clinical trial processes ICHGCP and global regulatory requirements
  • Clinical data standards (CDISC SDTM ADaM) and data governance practices
  • NonEDC data sources and data integration processes
• Strong organizational problemsolving 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 Mexico

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