Global Clinical Trials Lead - Renal/Obesity/MASH

IQVIA

Paris

Sur place

EUR 110 000 - 170 000

Plein temps

14 jours+
Générateur de candidature

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Avantages offerts par ce poste

Résumé du poste

IQVIA is seeking a Senior Project Manager to lead complex global clinical studies from start-up to close-out, ensuring quality, timelines and budgets align with sponsor objectives.

You will partner with sponsors and cross-functional teams across regions, driving proactive risk management, regulatory compliance and high-performance delivery of renal, obesity and MASH studies. This role offers leadership impact within a world-leading CRO and clinical research organization.

Qualifications

  • Bachelor's degree in Life Sciences or related field.
  • 7+ years of clinical research, including global/multi-regional trials.
  • Experience leading renal, obesity and/or MASH studies preferred.
  • Strong knowledge of ICH-GCP and regulatory requirements.
  • Proven ability to manage senior stakeholders and cross-functional teams.
  • Excellent leadership and communication skills.

Responsabilités

  • Lead delivery of complex global clinical studies from start-up to close-out.
  • Act as primary strategic partner for sponsors with leadership and innovative solutions.
  • Guide cross-functional teams across regions to ensure on-time, on-budget delivery.
  • Monitor timelines, budgets, quality, risks, and performance.
  • Drive risk management and issue resolution throughout study lifecycle.
  • Ensure compliance with ICH-GCP and regulatory contractual commitments.

Connaissances

Project management
Stakeholder management
Leadership
Cross-functional leadership
Risk management
Communication

Formation

Bachelor's degree in Life Sciences, Healthcare or related field

Description du poste

IQVIA is seeking a Senior Project Manager to lead complex global clinical studies from start-up to close-out, ensuring quality, timelines and budgets align with sponsor objectives.

You will partner with sponsors and cross-functional teams across regions, driving proactive risk management, regulatory compliance and high-performance delivery of renal, obesity and MASH studies. This role offers leadership impact within a world-leading CRO and clinical research organization.

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