12 дней назад
CRA 2 (Oncology)
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
CRA 2 (Oncology) (Clinical Research): Monitoring and managing clinical trial sites in São Paulo, Brazil, with an accent on oncology studies, GCP compliance, site performance, and data integrity. Focus on conducting site visits, supporting recruitment, maintaining TMF and ISF documentation, and resolving protocol and regulatory issues.
Location: São Paulo, Brazil
Company
IQVIA Biotech is a full-service contract research organization serving biotech sponsors with clinical research and healthcare intelligence solutions.
What you will do
- Conduct site selection, initiation, monitoring, and close-out visits in accordance with the study scope, GCP, and ICH guidelines.
- Collaborate with site staff on subject recruitment strategies, enrollment targets, protocol training, and issue resolution.
- Assess site performance, protocol adherence, regulatory submissions, CRF completion, and data-query resolution.
- Collect and maintain essential documents in the Trial Master File and Investigator Site File.
- Document site activities, visit outcomes, follow-up actions, and correspondence.
- Support cross-functional study execution, site-level recruitment planning, invoice collection, and budget tracking when required.
Requirements
- Bachelor’s degree in life sciences or a health-related field, or equivalent experience.
- At least 1 year of on-site monitoring experience in oncology.
- Strong understanding of GCP, ICH guidelines, and regulatory requirements.
- Ability to travel as required by the project.
Culture & Benefits
- Full-time employment.
- Work on clinical research programs supporting the development of medical treatments.
- Collaboration with cross-functional project teams and clinical sites.
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