Назад
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1 час назад

Senior Site Management Lead

124 500 - 236 500$
Формат работы
hybrid
Тип работы
fulltime
Грейд
senior/lead
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
Senior Site Management Lead (Clinical Research): Leading study-level clinical site management strategy and deliverables from study planning through closeout with an accent on site monitoring, engagement, compliance, and milestone execution. Focus on coordinating global study resources, mitigating operational risks, maintaining inspection readiness, and ensuring quality across clinical trial sites.

Location: Hybrid role based in North Chicago, Illinois, United States

Salary: $124,500–$236,500 per year

Company

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

What you will do

  • Lead study-level Clinical Site Management strategy and remain accountable for deliverables from planning through closeout.
  • Analyze study timelines, assumptions, milestones, and resource requirements to ensure feasible execution.
  • Set site monitoring and site engagement strategies and coordinate site selection, activation, adherence, engagement, and closure.
  • Oversee monitoring activities, quality deliverables, status tracking, milestone adherence, data snapshots, and database locks.
  • Identify, assess, and mitigate study risks while coordinating action plans with Site Management Leads and clinical study stakeholders.
  • Ensure site compliance, Clinical Site Management documentation, TMF completeness, and inspection readiness throughout the study.

Requirements

  • Bachelor’s degree or equivalent degree, typically in a paramedical or scientific field.
  • At least 7 years of clinical research industry experience, including 2 years in monitoring or project management and at least 1 year of global project management experience.
  • Experience managing components of global clinical trials and applying standard operating procedures, ICH guidelines, global regulations, ethics, and compliance requirements.
  • Fluency in English required.
  • Strong communication, leadership, planning, organizational, and stakeholder-influence skills in a matrix environment.
  • Advanced proficiency in Microsoft Word, PowerPoint, Excel, and OneNote.

Nice to have

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

Culture & Benefits

  • Paid vacation, holidays, and sick leave.
  • Medical, dental, and vision insurance for eligible employees.
  • 401(k) benefits for eligible employees.
  • Eligibility to participate in long-term incentive programs.
  • Work in a dynamic, fast-paced, collaborative, and matrixed environment.

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