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3 дня назад

Site Management Lead (Clinical Research)

109 500 - 208 500$
Формат работы
onsite
Тип работы
fulltime
Грейд
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
Site Management Lead (Clinical Research): Leading global and area-level clinical site management deliverables across study planning, site execution, monitoring, and closeout with an accent on study strategy, site engagement, compliance, and milestone delivery. Focus on managing monitoring plans, mitigating operational risks, maintaining inspection readiness, and coordinating site monitors and clinical study stakeholders in a matrix environment.

Location: Irvine, California, United States

Salary: $109,500–$208,500 per year

Company

hirify.global develops medicines and solutions for serious health conditions across immunology, oncology, neuroscience, and aesthetics.

What you will do

  • Lead global and/or area-level Clinical Site Management deliverables, timelines, resources, and milestones for assigned studies.
  • Develop study-level site monitoring plans and lead site engagement strategies.
  • Drive site activities from selection and activation through engagement, protocol adherence, data snapshots, database locks, and closeout.
  • Oversee monitoring activities, status tracking, quality deliverables, and milestone acceleration in collaboration with other Site Management Leads.
  • Identify, assess, and mitigate study risks; contribute to risk assessment and mitigation planning.
  • Maintain Clinical Site Management documentation, Trial Master File completeness, compliance, and inspection readiness throughout the study lifecycle.

Requirements

  • Bachelor’s degree or equivalent international degree, 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 across study phases; exposure to Phase II and III studies is preferred.
  • Knowledge of standard operating procedures, ICH requirements, global regulations, ethics, and compliance.
  • Strong communication, leadership, planning, organizational, presentation, and influencing skills in a matrix environment.
  • Fluency in English is required. Advanced proficiency in Microsoft Word, PowerPoint, Excel, and OneNote is expected.

Culture & Benefits

  • Full-time employment with 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.
  • Equal-opportunity workplace focused on integrity, innovation, and improving patient lives.

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