Key Facts

Remote From:

Mexico

Category: Data Manager

Full time

Mid-level (2-5 years)

English

Hard Skills

Clinical Data Management Vendor Management Data Integration Data Integrity Regulatory Compliance Data Quality Project Coordination Auditing Information Lifecycle Management Risk Analysis +9 more

Other Skills

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Timelines
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Communication
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Organizational Skills
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Detail Oriented
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Mentorship
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Problem Solving

Roles & Responsibilities

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, and clinical data standards (CDISC, SDTM, ADaM) with data governance practices
Education BS/BA required, preferably in Life Sciences, Health, Technology, or equivalent experience

Requirements:

Support end-to-end acquisition of third-party (non-EDC) clinical data for assigned studies and ensure data integrity, quality, compliance, and audit readiness
Collaborate with external vendors to align on timelines, processes, and issue resolution; monitor data deliverables and proactively identify and resolve risks or inconsistencies
Partner with cross-functional study teams to support study objectives; represent ACDM activities in study team meetings, audits, and inspections
Contribute to process improvements, data integration optimization initiatives, and provide informal training to coordinators and peers on study- and vendor-specific considerations

Job description

Associate Clinical Data Manager (ACDM)

Based in Mexico (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 Mexico 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, and inspections
Support and informally train coordinators and peers on study and vendor‑specific considerations
Contribute to process improvements and data integration optimization initiatives

What you bring

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