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13 часов назад

Site Management Lead (Clinical Research)

109 500 - 208 500$
Формат работы
onsite
Тип работы
fulltime
Грейд
lead
Английский
c1
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
Site Management Lead (Clinical Research): Directing global and area-level clinical site management deliverables across study planning, site activation, monitoring, data snapshots, database locks, and closeout with an accent on quality, timelines, resource alignment, and inspection readiness. Focus on leading site monitoring and engagement strategies, mitigating study-level risks, coordinating matrix stakeholders, and maintaining compliance across complex clinical trials.

Location: North Chicago, Illinois, United States; Irvine, California, United States

Salary: $109,500–$208,500 per year

Company

hirify.global discovers and delivers innovative medicines and solutions across areas including immunology, oncology, neuroscience, and aesthetics.

What you will do

  • Direct global and/or area-level Clinical Site Management deliverables, resources, timelines, and milestones across assigned studies.
  • Define and lead site monitoring and site engagement strategies, including Site Monitoring Plans.
  • Drive site-level activities from selection and activation through engagement, protocol adherence, monitoring, and closeout.
  • Oversee monitoring activities, status tracking, data snapshot and database lock deliverables, and site closure.
  • Identify, assess, and mitigate study risks while coordinating action plans with Clinical Study Team stakeholders.
  • Maintain CSM documentation, TMF completeness, site compliance, and inspection readiness throughout the study lifecycle.

Requirements

  • Bachelor’s degree or equivalent, typically in a paramedical or scientific field.
  • At least 5 years of industry clinical research experience, including 2 years in monitoring or project management, or equivalent experience on a global study.
  • Experience managing clinical trial components and applying standard operating procedures, ICH guidelines, global regulations, ethics, and compliance requirements.
  • Strong communication, leadership, planning, organization, presentation, and matrix collaboration skills.
  • Fluent English is required.
  • Advanced proficiency in Microsoft Word, PowerPoint, Excel, and OneNote.

Nice to have

  • Experience across study initiation through completion in multiple phases, including Phase II and III and Phase I in patients.
  • Experience across multiple therapeutic areas or disease indications.

Culture & Benefits

  • Benefits may include paid vacation, holidays, and sick leave.
  • Eligible employees may receive medical, dental, and vision insurance.
  • Eligible employees may participate in a 401(k) plan.
  • The role is eligible for long-term incentive programs.
  • Work takes place in a dynamic, fast-paced, matrix environment with opportunities to work both collaboratively and autonomously.

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