9 дней назад
Assoc. Central Monitor or Central Monitor (French Speaker)
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Assoc. Central Monitor or Central Monitor (French Speaker) (Clinical Monitoring): Performing centralized monitoring and reviewing structured clinical data and medical charts for multiple clinical trial projects with an accent on study quality, data integrity, and site oversight. Focus on managing monitoring triggers, investigating patient-level data, analyzing trends, and coordinating issue resolution with sites, CRAs, and cross-functional study teams.
Location: Home-based; candidates must be based in Argentina, Brazil, Mexico, Peru, Colombia, or Chile
Company
provides clinical research services, commercial insights, and healthcare intelligence for the life sciences and healthcare industries.
What you will do
- Perform centralized monitoring activities across assigned clinical trial projects, sites, and countries.
- Evaluate study quality and data integrity against protocols, SOPs, regulations, and guidelines.
- Manage monitoring triggers and prepare site information packages for assigned studies.
- Review structured clinical data, medical charts, and subject-level information, escalating issues that require further investigation.
- Perform trend analytics, maintain project systems and tracking tools, and support data issue triage.
- Collaborate with study teams, sites, and CRAs from project start through closeout.
Requirements
- Must be based in Argentina, Brazil, Mexico, Peru, Colombia, or Chile.
- Bachelor's degree in life sciences or a related field, nursing qualification, or near completion of the required degree.
- For the Central Monitor role: more than 2 years of monitoring experience, either onsite or remote.
- For the Associate Central Monitor role: more than 2 years of study coordinator experience.
- Advanced English and French are mandatory; both languages will be evaluated.
- Advanced Excel skills.
Culture & Benefits
- Home-based remote work arrangement.
- Support clinical trial sites in North America and potentially Latin America.
- Collaboration with cross-functional international study teams.
- Full-time employment.
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