7 дней назад
Sr CTA - Sponsor Dedicated - Israel
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
Sr CTA - Sponsor Dedicated - Israel (Clinical Research): Supporting clinical teams with accurate Trial Master File maintenance, clinical documentation, supplies, and data-flow tracking with an accent on regulatory compliance and study-file completeness. Focus on coordinating CRAs and Regulatory and Start-Up teams, managing Case Report Forms and queries, and maintaining project communications.
Location: Netanya, Israel
Company
provides clinical research services, commercial insights, and healthcare intelligence for the life sciences and healthcare industries.
What you will do
- Maintain accurate clinical documents and systems, including Trial Master Files, within project timelines.
- Support CRAs and Regulatory and Start-Up teams with the preparation, distribution, filing, and archiving of clinical documentation and reports.
- Review study files periodically for completeness and support site compliance tracking.
- Coordinate Clinical Trial Supplies, Case Report Forms, queries, and clinical data-flow tracking.
- Act as a central contact for designated project communications, correspondence, and related documentation.
- Accompany CRAs on site visits and assist with clinical monitoring duties after completing required training.
Requirements
- High School Diploma or equivalent.
- 3–4 years of previous Clinical Trial Associate experience.
- At least one year of clinical research experience is strongly preferred.
- Working knowledge of Microsoft Word, Excel, and PowerPoint.
- Good written and verbal command of English.
- Knowledge of Good Clinical Practice and International Conference on Harmonization guidelines, applicable protocol requirements, and strong organizational and communication skills.
Culture & Benefits
- Full-time employment in a clinical research environment.
- Collaboration with CRAs, Regulatory and Start-Up teams, managers, coworkers, and clients.
- Training provided on applicable clinical research regulations and protocol requirements.
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 →