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4 дня назад

Associate Director Study Start-up

182 145 - 212 860$
Формат работы
remote (только USA)
Тип работы
fulltime
Грейд
director
Английский
b2
Страна
US
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 Start-up (Clinical Trials/Pharma): Leading global study start-up planning and execution across a clinical trial portfolio with an accent on compliant delivery, operational readiness, and team leadership. Focus on managing Study Start-up Managers, monitoring portfolio performance and risks, and improving processes in line with ICH-GCP and regulatory requirements.

Location: United States - Remote

Annual base salary: $182,145–$212,860

Company

hirify.global is a biotechnology company developing and delivering medicines for serious diseases across oncology, inflammation, general medicine, and rare disease.

What you will do

  • Lead and manage Study Start-up Managers across multiple clinical programs and therapeutic areas.
  • Drive end-to-end study start-up planning and execution from global to local level.
  • Oversee portfolio performance, resourcing, delivery metrics, milestones, budgets, and risks.
  • Build team capability through coaching, mentoring, performance management, and best-practice modelling.
  • Partner with functional and hub leaders to strengthen study start-up capabilities and operational readiness.
  • Own study start-up business processes and lead training, knowledge sharing, and continuous improvement.

Requirements

  • Expertise in pharmaceutical clinical trial processes and operations.
  • Experience leading and managing global teams, with project management experience.
  • At least 3 years of direct people management or leadership experience involving teams, projects, programs, or resource allocation.
  • Clinical execution experience required by education level: 3 years with a doctorate, 7 years with a master’s degree, 9 years with a bachelor’s degree, 12 years with an associate’s degree, or 14 years with a high school diploma/GED.
  • Experience in life sciences and clinical trial work; no prior Veeva experience is required.

Nice to have

  • Seven years of life sciences experience, including five years of biopharmaceutical clinical research experience at a biotech or pharmaceutical company.
  • Experience managing multiple teams or direct reports across multiple clinical functions.

Culture & Benefits

  • Collaborative, innovative, science-based work environment.
  • Health, dental, vision, life, disability, and flexible spending benefits.
  • Retirement and savings plan with company contributions.
  • Annual bonus program and stock-based long-term incentives.
  • Paid time off, company-wide shutdowns, and flexible work models including remote arrangements where possible.

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