Plus
Включить Plus
Назад
Company hidden
15 дней назад

Freelance Clinical Research Associate (Oncology)

Формат работы
onsite
Тип работы
parttime
Грейд
middle
Английский
c1
Страна
CR
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
Для мэтча и отклика нужен Plus

Мэтч & Сопровод

Для мэтча с этой вакансией нужен Plus

Описание вакансии

Текст:
/
TL;DR
Freelance Clinical Research Associate (Oncology) (Clinical Trials): Supporting two Phase III oncology clinical trials through site evaluations, initiations, monitoring, close-outs, and compliance oversight with an accent on GCP compliance, data integrity, and investigator collaboration. Focus on conducting site visits, resolving study issues, tracking investigational product documentation, and maintaining audit and inspection readiness.

Location: Czech Republic; travel required to sites in Brno, Prague, Ostrava, and Hradec Kralove

FTE: 0.5; part-time freelance engagement lasting around five months, with potential extension.

Company

IQVIA provides clinical research services, commercial insights, and healthcare intelligence for the life sciences and healthcare industries.

What you will do

  • Support two Phase III oncology clinical trials.
  • Conduct site evaluations, initiations, monitoring visits, and close-outs.
  • Ensure GCP compliance, data integrity, and audit readiness.
  • Collaborate with investigators and internal teams while supporting site staff with training and issue resolution.
  • Review protocols, study manuals, and eCRFs.
  • Track investigational product inventory and documentation, attend investigator meetings, and support inspections.

Requirements

  • At least two years of CRA experience, including site monitoring.
  • Experience in oncology or hematology.
  • Strong knowledge of clinical trial processes and GCP.
  • Excellent communication and organizational skills, with the ability to work independently and manage priorities.
  • Fluent Czech and English required.

Culture & Benefits

  • Work with a clinical research team supporting the development of innovative medical treatments.
  • Immediate start available.
  • Part-time workload at 0.5 FTE.
  • Potential extension beyond the initial engagement period.

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 →