Назад
Company hidden
14 часов назад

Associate Director Global Clinical Program

Формат работы
onsite
Тип работы
fulltime
Грейд
director
Английский
b2
Страна
US
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
Для мэтча и отклика нужен Plus

Мэтч & Сопровод

Для мэтча с этой вакансией нужен Plus

Описание вакансии

Текст:
/
TL;DR
Associate Director Global Clinical Program (Clinical Research): Leading the operational delivery of multiple complex clinical studies and programs with an accent on timelines, budgets, quality, risk management, and patient-centric execution. Focus on coordinating global teams and vendors, guiding study design and country selection, managing program-level escalations, and developing Study Delivery Leads.

Location: US - California - Thousand Oaks

Company

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

What you will do

  • Lead operational planning and delivery for multiple clinical studies and programs, ensuring timelines, budgets, quality, and strategy are met.
  • Identify delivery risks, manage program-level issues and escalations, and guide corrective actions.
  • Drive consistent operational practices and continuous improvement across assigned studies.
  • Line-manage and develop Study Delivery Leads.
  • Partner with cross-functional and local execution teams on priorities, resources, study design, country selection, enrolment, diversity, and patient-centric approaches.
  • Manage program budgets, vendors, forecasting, and external clinical research providers.

Requirements

  • Doctorate degree and 3 years of clinical execution experience, or a relevant lower degree with the corresponding required experience: 7 years for a master’s, 9 years for a bachelor’s, 12 years for an associate’s degree, or 14 years with a high school diploma/GED.
  • At least 3 years of direct people management or leadership experience involving teams, projects, programs, or resource allocation.
  • Preferred: 8 years in life sciences or a medically related field, including 6 years of biopharmaceutical clinical research experience.
  • Experience managing multiple teams or direct reports across multiple geographies.
  • Experience overseeing CROs, central laboratories, imaging vendors, or other clinical research vendors.

Culture & Benefits

  • Collaborative, innovative, and science-based working 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.
  • Time-off plans, company-wide shutdowns, and career development opportunities.
  • Flexible work models, including remote arrangements where possible.

Будьте осторожны: если работодатель просит войти в их систему, используя iCloud/Google, прислать код/пароль, запустить код/ПО, не делайте этого - это мошенники. Обязательно жмите "Пожаловаться" или пишите в поддержку. Подробнее в гайде →