14 дней назад
Senior CRA
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Senior CRA (Clinical Research): Managing clinical trial site selection, initiation, monitoring, close-out, documentation, and recruitment activities with an accent on GCP compliance, data integrity, and regulatory requirements. Focus on tracking submissions, recruitment, CRF completion, and data query resolution while evaluating site quality and coordinating study training.
Location: Buenos Aires, Argentina
Company
provides clinical research services, commercial insights, and healthcare intelligence for the life sciences and healthcare industries.
What you will do
- Perform site selection, initiation, monitoring, and close-out visits while maintaining required documentation.
- Support subject recruitment planning and track recruitment progress.
- Establish communication with assigned sites and deliver protocol and study-related training.
- Evaluate site practices and data quality, escalating quality issues when appropriate.
- Track regulatory submissions, CRF completion, and data query resolution.
- Collaborate with colleagues and customers across clinical research projects.
Requirements
- Bachelor’s degree in healthcare, a scientific discipline, or an equivalent qualification.
- At least 4 years of on-site monitoring experience.
- Advanced English proficiency.
- In-depth knowledge of GCP, ICH guidelines, and applicable regulatory requirements.
- Strong organizational, time-management, communication, and interpersonal skills, with the ability to work independently and in a team.
- Proficiency with clinical trial management systems and electronic data capture systems; willingness to travel as required.
Culture & Benefits
- Work on clinical research projects intended to improve patient health and population outcomes.
- Collaborate with colleagues, customers, and clinical trial sites.
- Travel to sites as required by assigned studies.
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