Senior Clinical Trial Contract Analyst (Hybrid)

10 John C. Lincoln Medical Center

Phoenix (AZ)

Hybride

USD 90 000 - 130 000

Plein temps

Il y a 4 jours
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Résumé du poste

HonorHealth is seeking an experienced Clinical Trial Contract Analyst III to lead complex negotiations and minimize institutional risk while growing research initiatives in Arizona. This senior role mentors staff, advocates best practices, and partners with finance, compliance and legal to streamline templates and processes.

The candidate will oversee high-value agreements, engage with sponsors and CROs, and drive faster activation of trials while maintaining rigorous risk controls in a hybrid

Qualifications

  • 5 years with at least 2 years in a senior or lead role in clinical trial contract negotiation or research administration.
  • Experience mentoring junior staff and leading negotiations for high-value agreements.
  • Strong negotiation, policy development, and template refinement experience.

Responsabilités

  • Lead negotiations for complex, high-value or novel clinical trial contracts.
  • Provide expert advice on contract strategy and risk mitigation.
  • Manage sponsor and CRO relationships to improve contract turnaround times.
  • Mentor and train junior analysts on advanced negotiation practices.
  • Collaborate with finance, compliance and legal to refine templates and workflows.

Connaissances

Contract negotiations
Team leadership
Stakeholder management
Regulatory compliance

Formation

Bachelors in Business Administration
Masters in Healthcare Administration
Juris Doctor (JD) preferred

Description du poste

HonorHealth is seeking an experienced Clinical Trial Contract Analyst III to lead complex negotiations and minimize institutional risk while growing research initiatives in Arizona. This senior role mentors staff, advocates best practices, and partners with finance, compliance and legal to streamline templates and processes.

The candidate will oversee high-value agreements, engage with sponsors and CROs, and drive faster activation of trials while maintaining rigorous risk controls in a hybrid

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