11 дней назад
Freelance CRA (Clinical Research) - Spain
Вакансия из Hirify Global, списка международных tech-компанийДля мэтча и отклика нужен Plus
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Freelance CRA (Clinical Research) - Spain (Phase III Clinical Trials): Monitoring Phase III clinical studies across approximately 10 sites in Spain with an accent on interim monitoring visits, protocol adherence, ICH-GCP compliance, and source document verification. Focus on identifying and following up on site issues, supporting investigators, and coordinating with project teams during a six-month assignment.
Location: Spain, with nationwide travel and approximately 2–3 site visits per month. The role is based in Barcelona and supports approximately 10 clinical trial sites across Spain.
Company
provides clinical research services, commercial insights, and healthcare intelligence for the life sciences and healthcare industries.
What you will do
- Perform Interim Monitoring Visits at clinical trial sites.
- Ensure protocol adherence and ICH-GCP compliance.
- Verify source documents and study data.
- Support investigators and site personnel.
- Identify and follow up on site issues and action plans.
- Collaborate with project teams to support successful study delivery.
Requirements
- At least 2 years of CRA monitoring experience.
- Previous Phase III clinical trial experience.
- Strong knowledge of ICH-GCP and clinical trial processes.
- Ability to work independently with excellent communication and organizational skills.
- Fluent Spanish and English.
- Willingness to travel throughout Spain.
Culture & Benefits
- Freelance, part-time assignment of approximately 0.5 FTE, or 18 hours per week.
- Approximately six-month engagement starting as soon as possible.
- Opportunity to support two Phase III clinical studies in Spain.
- Two freelance CRA openings are available, with assignments potentially combinable depending on availability and project needs.
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