Senior Phase I Clinical Trial Leader

IQVIA Argentina

Amsterdam

On-site

EUR 90,000 - 130,000

Full time

6 days ago
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Job summary

IQVIA is seeking a Clinical Trial Leader / Senior Clinical Trial Leader to oversee Phase I Healthy Volunteer studies from preparation through reporting, ensuring participant safety and high-quality delivery. The role requires strong leadership across interdisciplinary teams and alignment with medical and pharmacology partners.

You will shape study design, contribute to dose-escalation decisions, and manage governance and risk in a fast-paced, sponsor-dedicated setting within the Clinical FSP

Qualifications

  • Recent Phase I Healthy Volunteer leadership with end-to-end accountability.
  • Strong knowledge of early phase study designs and protocol authoring.
  • Ability to interpret PK/PD data and support dose-escalation decisions.

Responsibilities

  • Provide leadership to trial teams and maintain accountability for end-to-end Phase I Healthy Volunteer studies.
  • Contribute to study design, protocol development, and governance across cross-functional partners.
  • Oversee safety, quality, milestones and budget adherence throughout the trial lifecycle.
  • Coordinate with medical, pharmacology and statistics teams to ensure compliant, timely delivery.

Skills

End-to-end leadership
Protocol design
Clinical pharmacology
Dose escalation
Risk management
Cross-functional collaboration
Communication
GCP/ICH knowledge
English fluency

Education

Master’s degree or higher in life sciences/related

Tools

CTMS
eTMF

Job description

IQVIA is seeking a Clinical Trial Leader / Senior Clinical Trial Leader to oversee Phase I Healthy Volunteer studies from preparation through reporting, ensuring participant safety and high-quality delivery. The role requires strong leadership across interdisciplinary teams and alignment with medical and pharmacology partners.

You will shape study design, contribute to dose-escalation decisions, and manage governance and risk in a fast-paced, sponsor-dedicated setting within the Clinical FSP

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