11 дней назад
Clinical Research Associate II (Clinical Research)
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
Clinical Research Associate II (Clinical Research): Monitoring clinical study sites from selection through close-out, supporting recruitment, training, regulatory submissions, data queries, documentation, and site finances with an accent on GCP compliance, site quality, and study execution. Focus on conducting on-site monitoring, resolving complex operational issues, and maintaining regulatory and financial control across clinical trials.
Location: Auckland, New Zealand. Candidates must have full work rights in New Zealand; visa sponsorship is not available.
Company
is a global contract research organization providing clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries.
What you will do
- Conduct site visits from selection through study close-out.
- Develop and implement recruitment strategies for study subjects.
- Train study sites and maintain effective communication with site personnel.
- Monitor protocol compliance, regulatory submissions, data queries, and study progress.
- Maintain complete site documentation and oversee site financials and invoice retrieval.
- Collaborate with project teams, managers, coworkers, and clients to support study execution.
Requirements
- Bachelor’s degree in a scientific or healthcare discipline preferred.
- At least four years of on-site clinical study monitoring experience.
- Strong knowledge of GCP and ICH guidelines.
- Experience with Microsoft Office and relevant clinical research technology.
- Strong written and verbal communication, organization, analytical, problem-solving, time-management, and financial-management skills.
- Full work rights in New Zealand are required; visa sponsorship is not available.
Nice to have
- Experience in oncology and haematology trials.
Culture & Benefits
- Stability and resources of a leading global contract research organization.
- Direct experience supporting a customer’s clinical research programs.
- Access to world-class training and mentoring.
- Opportunity to gain experience across a wide range of therapeutic areas.
Hiring process
- Completion of a short video screening is required as part of the interview process.
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