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22 часа назад

Associate Director, Study Operations, Rater Services (Clinical Research)

Формат работы
onsite
Тип работы
fulltime
Грейд
director
Английский
b2
Страна
CR
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Описание вакансии

Текст:
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TL;DR
Associate Director, Study Operations, Rater Services (Clinical Research): Leading Cronos study operations and project governance from initiation through closeout with an accent on clinical research compliance, resource allocation, and team development. Focus on managing project risks, escalating issues, improving operational processes, and ensuring accurate delivery of financial and study documentation.

Location: Prague, Czech Republic

Company

IQVIA provides clinical research services, commercial insights, and healthcare intelligence for the life sciences and healthcare industries.

What you will do

  • Serve as the Principal or Person in Charge for Cronos projects, leading initiation, execution, and closeout.
  • Oversee project governance, regulatory compliance, risk assessments, issue escalation, and governance reviews.
  • Lead, mentor, and develop Project Managers and Project Manager Analysts.
  • Allocate resources and balance workloads across multiple projects.
  • Ensure timely completion of deliverables, including financial reconciliation, documentation, and archiving.
  • Drive process improvement, operational excellence, strategic initiatives, and business development support.

Requirements

  • Bachelor’s degree in life sciences, business, or a related field; a Master’s degree is preferred.
  • 7+ years of experience in clinical research, project management, or study operations, including at least 3 years in a leadership role.
  • Experience with project governance, risk management, process improvement, and team management.
  • Strong communication, problem-solving, stakeholder management, and organizational skills.
  • Computer proficiency, including Microsoft Office; experience with Smartsheet, SAP, or SharePoint is preferred.
  • Strong commitment to quality and continuous improvement.

Culture & Benefits

  • Full-time employment.
  • Work in a clinical research and healthcare intelligence environment.
  • Collaboration with cross-functional teams and senior management.

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