обновлено 2 дня назад
Pharmacovigilance Specialist
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Pharmacovigilance Specialist (Clinical Safety): Processing and assessing safety data, adverse events, endpoint information, and literature-related activities with an accent on regulatory compliance, medical coding, and accurate database entry. Focus on determining event status, writing narratives, tracking incoming reports, and coordinating safety issues with internal teams and healthcare professionals.
Location: Mexico City, Mexico; 100% home-based
Company
IQVIA provides clinical research services, commercial insights, and healthcare intelligence for the life sciences and healthcare industries.
What you will do
- Review, assess, and process safety data from multiple sources in line with regulations, SOPs, guidelines, and project requirements.
- Collect and track incoming adverse events and endpoint information.
- Determine initial or update status, enter data into databases, and code adverse events and products.
- Write case narratives and perform literature-related pharmacovigilance 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 and Spanish is mandatory.
- Ability to follow applicable regulations, guidelines, SOPs, and internal procedures.
- Up to 3 years of previous clinical experience is desirable.
- Pharmacovigilance experience is valued, particularly at least 1 year.
Culture & Benefits
- 100% home-based work modality.
- Work within a global clinical research and healthcare intelligence organization.
- Role supporting the development and commercialization of medical treatments and improved patient outcomes.
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