Senior Clinical Project Lead — Global Trials & Delivery

IQVIA Inc

Lisboa

Hybrid

EUR 85,000 - 120,000

Full time

44 hours ago
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Job summary

IQVIA Inc in Lisbon seeks a Senior Clinical Project Manager to lead multi-country clinical studies, direct the core project team and ensure on-time delivery to contract, SOPs and quality standards. You will partner with clients and internal functions to optimize timelines, budgets and study quality, while mentoring junior staff and advancing operational excellence.

Strong leadership, communication and regulatory knowledge are essential to deliver high-impact trials and drive patient outcomes in

Qualifications

  • Bachelor's Degree Life sciences or related field.
  • 7+ years clinical research experience including 4+ years project management experience.
  • Knowledge of clinical trials conduct and regulatory requirements (ICH GCP, local laws).
  • Strong written and verbal communication skills in English.
  • Leadership and cross-functional collaboration capabilities.

Responsibilities

  • Lead bid defense preparations and presentations with Business Development.
  • Develop integrated study management plans with core project team.
  • Oversee strategic planning and execution of studies per contract, SOPs and quality standards.
  • Set objectives for core project team and monitor performance.
  • Identify and manage risks, issues and change control; drive continuous improvement.

Skills

Clinical research
Project management
English communication
Leadership
Problem solving

Education

Bachelor's Degree Life sciences

Tools

MS Word
MS Excel
PowerPoint
MS Office

Job description

IQVIA Inc in Lisbon seeks a Senior Clinical Project Manager to lead multi-country clinical studies, direct the core project team and ensure on-time delivery to contract, SOPs and quality standards. You will partner with clients and internal functions to optimize timelines, budgets and study quality, while mentoring junior staff and advancing operational excellence.

Strong leadership, communication and regulatory knowledge are essential to deliver high-impact trials and drive patient outcomes in

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