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6 дней назад

Study Delivery Senior Manager (Study Delivery Lead)

163 721 - 197 116$
Формат работы
remote (только USA)
Тип работы
fulltime
Грейд
senior
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
Study Delivery Senior Manager (Study Delivery Lead) (Clinical Trials): Leading end-to-end global clinical trial delivery, from feasibility and site selection through enrollment, data flow, monitoring, and vendor execution, with an accent on quality, timelines, budget, participant safety, and data integrity. Focus on designing study plans, managing cross-functional teams and global vendors, resolving complex operational risks, and ensuring regulatory compliance.

Location: United States - Remote

Salary: $163,721–$197,116 USD annually

Company

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

What you will do

  • Own end-to-end delivery of assigned global clinical studies, including quality, timelines, budget, and operational performance.
  • Lead cross-functional study teams and align delivery with evidence-generation strategies.
  • Define study plans covering feasibility, site selection, site engagement, recruitment, retention, and vendor delivery.
  • Oversee enrollment, data flow, monitoring, corrective actions, and study execution across geographies.
  • Identify and manage study risks using quality-by-design and risk-based approaches to protect participant safety and data integrity.
  • Partner with internal stakeholders and external vendors while driving continuous improvement, innovation, and regulatory compliance.

Requirements

  • Doctorate degree and 2 years of Clinical Execution experience, or master’s degree and 4 years, bachelor’s degree and 6 years, associate’s degree and 10 years, or high school diploma/GED and 12 years.
  • Experience leading global clinical trials in a biotech, pharmaceutical, or CRO organization.
  • Experience managing direct reports across multiple geographies.
  • Experience representing a sponsor company in regulatory audits or inspections.
  • Experience overseeing clinical research vendors, including CROs, central labs, or imaging vendors.

Nice to have

  • 7 years of experience in life sciences or a medically related field, including 5 years in biopharmaceutical clinical research.

Culture & Benefits

  • Health, dental, vision, life, disability, and flexible spending benefits.
  • Retirement and savings plan with company contributions.
  • Discretionary annual bonus program and stock-based long-term incentives.
  • Paid time-off plans and career development opportunities.
  • Flexible work models where applicable.

Hiring process

  • Sponsorship for this role is not guaranteed.
  • Reasonable accommodation is available during the application and interview process.

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