Senior Clinical Trial Lead: Global Biotech Trials

IQVIA Inc

Ciudad de México

On-site

MXN 900,000 - 1,200,000

Full time

2 days ago
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Job summary

IQVIA Biotech is seeking a Clinical Trial Manager II to lead clinical delivery for global studies from Mexico City. You will partner with cross-functional teams, ensure compliance with SOPs and regulatory requirements, and drive project milestones while managing budgets and risks.

The role requires 5+ years in clinical research, strong leadership, and excellent communication in English. Travel and collaboration with international sites are possible as part of delivering and optimizing trials.

Qualifications

  • Bachelor's Degree in health care or other scientific discipline required.
  • Requires 5+ years clinical research/monitoring experience.
  • Knowledge of GCP/ICH and regulatory requirements.
  • Strong communication in English (written and verbal).
  • Understanding of project finances and budgeting.

Responsibilities

  • Ensure clinical delivery of assigned projects in compliance with regulatory requirements (ICH/GCP).
  • Meet recruitment targets and implement recruitment strategies.
  • Contribute to project risk mitigation plans and manage clinical risks.
  • Monitor clinical quality and oversee related issues.
  • Manage project finances including Estimate at Completion (EAC).
  • Collaborate with clinical teams and stakeholders to meet milestones.

Skills

Project management
Leadership
Communication
Budget & finance
Risk management
Mentoring

Education

Bachelor's Degree in health care or science

Job description

IQVIA Biotech is seeking a Clinical Trial Manager II to lead clinical delivery for global studies from Mexico City. You will partner with cross-functional teams, ensure compliance with SOPs and regulatory requirements, and drive project milestones while managing budgets and risks.

The role requires 5+ years in clinical research, strong leadership, and excellent communication in English. Travel and collaboration with international sites are possible as part of delivering and optimizing trials.

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