1 день назад
Pharmacovigilance Specialist (Fluent in English + French)
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Pharmacovigilance Specialist (English/French/Spanish): Processing and assessing safety data, adverse events, endpoint information, and literature-related records with an accent on regulatory compliance, medical coding, and accurate database entry. Focus on determining event status, writing case narratives, tracking incoming reports, and coordinating safety issues with healthcare professionals and cross-functional teams.
Location: Mexico City, Mexico; 100% home-based
Company
Global provider of clinical research services, commercial insights, and healthcare intelligence for the life sciences and healthcare industries.
What you will do
- Process and assess safety data according to applicable regulations, guidelines, SOPs, and project requirements.
- Collect and track incoming adverse events and endpoint information.
- Determine the initial or update status of incoming events and enter cases into the database.
- Code adverse events and products, write case narratives, and perform literature-related activities.
- Maintain required quality, productivity, and delivery standards.
- Coordinate with functional team members 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 French is mandatory.
- English and French proficiency will be evaluated during the hiring process.
- Up to three years of previous clinical experience is desirable.
- One year of pharmacovigilance experience is highly valued.
Culture & Benefits
- Fully home-based work modality.
- Work aligned with applicable regulations, SOPs, and internal quality guidelines.
- Opportunity to contribute to clinical research and patient safety activities.
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