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Manager, Records Management (LATAM)

Precision Medicine Group
Latin America

  • Oversee Trial Master File (TMF) activities including document review, quality checks, and study-level engagement to ensure regulatory compliance.
  • Manage a team of Documents Specialists, Quality Review Specialists, and TMF Leads, providing training, performance management, and support.
  • Collaborate with leadership to drive process improvements and ensure efficient records management across clinical programs.

ETMF Regulatory Compliance Microsoft Office Leadership Clinical Research
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TMF Lead II (LATAM)

Precision Medicine Group
LATAM

  • Ensure timely review, processing, and quality of Trial Master Files (TMF) according to GCP and SOPs.
  • Create and execute study TMF plans, manage document indexing, and communicate changes to project teams.
  • Monitor TMF health, identify risks, and support audits and inspections for compliance.

Precision Medicine Group is a global contract research organization providing clinical trial support and precision medicine services. The company values professionalism, collaboration, and quality, with a focus on maintaining inspection-ready trial master files.

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