Global Data Management Lead for Clinical Trials

IQVIA LLC

Ciudad de México

Presencial

MXN 900.000 - 1.200.000

Jornada completa

Hace 4 días
Sé de los primeros/as/es en solicitar esta vacante
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Transforma esta oferta en una entrevista — un currículum y una carta de presentación creados pensando en lo que quiere el empleador.

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Descripción de la vacante

IQVIA LLC in Mexico City seeks an experienced Data Management leader to independently manage end-to-end delivery of data management services for global trials, ensuring quality, timeliness, and budget adherence.

You will provide leadership to the CDM team, engage with customers, drive process improvements, negotiate timelines and financials, and ensure compliance with GCP and regulatory guidelines throughout the DM lifecycle.

Formación

  • Bachelor's Degree Health, clinical, biological, or mathematical sciences; 7 years direct Data Management experience, including 5+ years as a CDM project lead.

Responsabilidades

  • Serve as primary point of contact for customer on data management deliverables.
  • Manage multiple large studies or programs (global).
  • Provide leadership to DTLs on global studies/programs.
  • Lead negotiations with customer on timelines, financials, processes.
  • Manage DM service delivery with DM process and technical expertise.
  • Review and sign-off on data management plan documents.
  • Ensure service and quality meet specifications per DMP and contract/SOW.

Conocimientos

CDM leadership
Data Management
GCP knowledge
Regulatory compliance
Contract negotiations
Stakeholder management
Clinical drug development
Communication
Team mentorship
Problem solving

Educación

Bachelor's Degree Health or biological sciences

Descripción del empleo

IQVIA LLC in Mexico City seeks an experienced Data Management leader to independently manage end-to-end delivery of data management services for global trials, ensuring quality, timeliness, and budget adherence.

You will provide leadership to the CDM team, engage with customers, drive process improvements, negotiate timelines and financials, and ensure compliance with GCP and regulatory guidelines throughout the DM lifecycle.

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