Senior Clinical Data Team Lead — Global Trials & DM

Velocehr

Buenos Aires

On-site

ARS 181,906,000 - 272,860,000

Full time

4 days ago
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Job summary

IQVIA is seeking a Senior Clinical Data Team Lead to manage end-to-end data management delivery for global studies. You will act as the primary client contact for DM deliverables, lead a team of DTLs, and ensure quality, timelines, and budgets across complex projects.

You will mentor junior staff, support bid defenses, and collaborate with cross-functional teams to optimize DM processes and regulatory compliance.

Qualifications

  • Bachelor's degree in health, clinical, biological, or mathematical sciences, or related field.
  • 7+ years direct Data Management experience, including 5+ years as a CDM project lead.
  • Experience delivering multiple global trials through full DM life cycle (large trials of 1000+ patients).
  • Demonstrated expert data management skills and advanced knowledge of the data management process.

Responsibilities

  • Serve as primary client contact for data management deliverables.
  • Manage multiple large studies or programs and provide leadership to DTLs.
  • Provide project management expertise with customer data managers and internal teams.
  • Lead negotiations with customers on timelines, financials, processes, resources.
  • Mentor junior staff and ensure timely completion of project activities.
  • Oversee DM service delivery with quality and compliance to contracts.

Skills

Data Management
CDM project lead
Project leadership
Client negotiations
Regulatory knowledge
GCP compliance

Education

Bachelor's degree in health/clinical/biological/mathematical sciences

Job description

IQVIA is seeking a Senior Clinical Data Team Lead to manage end-to-end data management delivery for global studies. You will act as the primary client contact for DM deliverables, lead a team of DTLs, and ensure quality, timelines, and budgets across complex projects.

You will mentor junior staff, support bid defenses, and collaborate with cross-functional teams to optimize DM processes and regulatory compliance.

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