26 дней назад
Medical Information and Adverse Event Intake Specialist (Pharmacovigilance)
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
Medical Information and Adverse Event Intake Specialist (Pharmacovigilance): Reviewing, assessing, and processing adverse event, product quality, and medical inquiry information for pharmaceutical safety databases with an accent on case triage, medical terminology coding, narrative writing, and quality control. Focus on handling complex safety data, coordinating translations, driving case closure, and supporting healthcare professionals and consumers in Estonian, English, and an additional language.
Location: Riga, Latvia
Company
IQVIA provides clinical research services, commercial insights, and healthcare intelligence for the life sciences and healthcare industries.
What you will do
- Provide phone and email support to healthcare professionals and consumers regarding adverse events, product quality complaints, medical inquiries, and product support.
- Receive, triage, review, and process lifecycle safety operational data.
- Enter and track data in lifecycle safety databases, code medical terminology, write case narratives, generate queries, and perform quality control.
- Assist with reconciliation, case closure, translations, and documentation of safety reports from investigative sites and other sources.
- Collaborate with lifecycle safety colleagues, project managers, clients, and operations teams to resolve issues and maintain effective service communications.
- Support training, mentoring, working groups, and implementation of new lifecycle safety initiatives.
Requirements
- Degree in life sciences.
- Native or C2-level Estonian, English, and at least C1 in an additional foreign language.
- Strong written and verbal communication skills, attention to detail, accuracy, organization, and time management.
- Ability to manage multiple projects, competing priorities, and independent workloads.
- Ability to establish effective working relationships with coworkers, managers, and clients.
- Willingness and aptitude to learn new skills across lifecycle safety service lines.
Culture & Benefits
- Opportunity to work as part of a global pharmaceutical safety services organization.
- Development opportunities toward oversight of projects and teams.
- Collaborative environment focused on product safety and patient outcomes.
- UK visa sponsorship is not available for this role.
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