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2 часа назад

Clinical Research Associate II

Формат работы
remote (только United_kingdom)
Тип работы
fulltime
Грейд
middle
Английский
b2
Страна
UK
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

Clinical Research Associate II: Monitoring and owning the progress of clinical studies at investigative sites, ensuring studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP, and applicable regulations with an accent on site setup/monitoring coordination and risk identification/mitigation. Focus on investigator and site activities (pre-study, initiation, site visits) and maintaining quality outcomes while handling conflict effectively.

Location: Remote (fully home based) in the United Kingdom or Northern Ireland

Company

hirify.global is a CRO focused on precision medicine, combining clinical trial operations with advanced biomarker and data analytics for oncology and rare diseases.

What you will do

  • Monitor and own clinical study progress at investigative sites, ensuring execution and reporting align with protocol, SOPs, ICH-GCP, and regulations.
  • Coordinate study setup and monitoring activities, including identifying investigators and supporting regulatory submissions.
  • Conduct pre-study and initiation visits and manage investigator meeting and site visit readiness.
  • Identify potential study risks and propose mitigation solutions to protect quality and outcomes.
  • Handle conflict using proven resolution strategies and maintain responsiveness when issues arise.

Requirements

  • Location eligibility: fully home based in the UK or Northern Ireland.
  • Fluency in English.
  • 4-year college degree or equivalent experience.
  • Ideally 1+ years CRA experience in a CRO or pharmaceutical industry.
  • Availability for domestic travel with overnight stays; travel may be ~50–60% (international travel may be required for some senior-level positions).
  • Oncology experience is desirable (early phase experience desirable, but not essential).

Culture & Benefits

  • Lower-than-average protocol volume to support protocol expertise and work/life balance.
  • Reasonable travel expectations and direct line management support.
  • Smaller CRO environment with input and influence on meaningful operational impact.
  • Emphasis on quality outcomes and retention through an enjoyable quality of life.

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