Назад
Company hidden
4 дня назад

Senior Clinical Research Associate (Clinical Trials)

Формат работы
remote (только Spain)
Тип работы
fulltime
Грейд
senior
Английский
c1
Страна
Spain
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
Senior Clinical Research Associate (Clinical Trials): Supporting 2–3 clinical trials through site start-up, monitoring, data verification, investigational product management, safety reporting, and study close-out with an accent on GCP compliance and reliable clinical data. Focus on conducting on-site and remote monitoring, coordinating sites, training investigators, resolving data queries, and supervising junior CRAs.

Location: Remote position based in Spain, with Barcelona as the ideal location; regular travel to clinical trial sites is required.

Company

hirify.global is a global full-service contract research organization providing clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies.

What you will do

  • Support 2–3 clinical trials across study start-up, monitoring, data review, and close-out.
  • Conduct site selection, evaluation, initiation, periodic monitoring, and termination visits both on-site and remotely.
  • Train site staff, act as the main site contact, and ensure timely follow-up of trial activities and documentation.
  • Perform source data verification, review CRFs and clinical data, and resolve data queries.
  • Manage investigational products, trial materials, investigator files, safety reporting, and study documentation.
  • Guide and supervise CRA I staff and support training, submissions, feasibility, and site budget activities.

Requirements

  • University degree in a scientific, medical, or paramedical discipline.
  • At least eight years of clinical research experience, including on-site monitoring as a CRA.
  • Previous experience working for a CRO is required.
  • Strong knowledge of clinical trial operations, GCP/ICH Guidelines, and applicable regulatory requirements.
  • Fluent English and Spanish are required.
  • Proficiency in Microsoft Office and willingness to travel.

Nice to have

  • Experience across a broad range of therapeutic areas.

Culture & Benefits

  • Full-time, permanent employment with a remote working arrangement based in Spain.
  • Professional development supported through continuous training and close management.
  • Collaborative one-team culture focused on quality and work-life balance.
  • Opportunity to work with pharmaceutical, biotechnology, medical device, and consumer health clients.
  • Inclusive and diverse work environment.

Hiring process

  • Submit a CV and receive an acknowledgement of receipt.
  • Qualified candidates are invited to a phone interview as the first step.

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 →