Clinical Research Associate II
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
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
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.
Будьте осторожны: если работодатель просит войти в их систему, используя iCloud/Google, прислать код/пароль, запустить код/ПО, не делайте этого - это мошенники. Обязательно жмите "Пожаловаться" или пишите в поддержку. Подробнее в гайде →