обновлено 2 дня назад
Data Manager for Clinical Trials
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
Data Manager for Clinical Trials (Clinical Data Management): Managing clinical and medical data, EDC databases, eCRFs, validation plans, and database activities for clinical research projects with an accent on data quality, regulatory readiness, and cross-functional coordination. Focus on designing data management documentation, reconciling safety data, coding medical data, and preparing databases for lock and audits.
Location: São Paulo, Brazil; candidates must be based in Brazil
Company
PSI is a privately owned, full-service contract research organization originating in Switzerland and supporting pharmaceutical clinical trials globally.
What you will do
- Track clinical database setup, testing, maintenance, data entry, validation, and database lock activities.
- Design eCRFs, data management plans, data validation plans, and study-specific guidelines.
- Review clinical data, perform manual CRF reviews, reconcile serious adverse events, and code medical data.
- Coordinate CRF and query processing, dispatch, archiving, and maintenance of clinical data management files.
- Communicate with clients, project teams, vendors, and site staff on data management matters.
- Perform database quality control checks, support audits, and train site and project teams.
Requirements
- College or university degree; a Life Science or Pharmacy background is relevant.
- Demonstrated experience managing clinical or medical data.
- Full working proficiency in English is required.
- Experience with clinical data management systems such as Medidata Rave or Oracle InForm.
- Proficiency with Microsoft Office applications.
- Strong organisational, time management, independent working, and multitasking skills.
Culture & Benefits
- Work within a global clinical research organization supporting projects across multiple countries and continents.
- Inclusive environment focused on welcoming and valuing colleagues from diverse backgrounds.
- Opportunity to contribute to pharmaceutical clinical research across a broad range of therapeutic indications.
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