18 часов назад
Operations Specialist (Pharmacovigilance)
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Operations Specialist (Pharmacovigilance): Processing and distributing safety data, adverse events, and endpoint information for clinical research services with an accent on regulatory compliance, pharmacovigilance workflows, and accurate database documentation. Focus on coding adverse events and products, writing narratives, conducting literature-related activities, and coordinating with healthcare professionals and functional teams.
Location: Buenos Aires, Argentina; 100% home-based
Company
provides clinical research services, commercial insights, and healthcare intelligence for the life sciences and healthcare industries.
What you will do
- Review, assess, process, and distribute safety data from multiple sources in line with regulations, SOPs, and project requirements.
- Collect and track incoming adverse events and endpoint information, determining whether events are initial or updated reports.
- Enter data into databases, code adverse events and products, write narratives, and perform literature-related activities.
- Maintain project quality, productivity, and delivery standards.
- Coordinate with functional teams and healthcare professionals to resolve project-related issues.
Requirements
- Bachelor’s degree in life sciences or a related field is mandatory.
- Fluency in English, Spanish, and Portuguese is required.
- English and Portuguese fluency will be evaluated.
- Knowledge of applicable regulations, guidelines, SOPs, and project requirements.
Nice to have
- Up to 3 years of previous clinical experience.
- At least 1 year of pharmacovigilance experience.
Culture & Benefits
- Fully home-based work modality.
- Work supporting the development and commercialization of medical treatments and improved patient outcomes.
- Integrity-focused hiring process with strict requirements for truthful and complete application information.
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