Operations Specialist 1
Aviso de fuente externaen IQVIA
IQVIA seeks an Operations Specialist 1 to process safety data and perform pharmacovigilance activities. English and Spanish fluency is mandatory.
Salario
No especificado
Ubicación
Buenos Aires, Argentina
Tipo de empleo
Tiempo completo
Modalidad
No especificado
Operations Specialist 1
Buenos Aires, Argentina
Descripción del empleo
About the role
At IQVIA, review, assess, and process safety data and information received from various sources across service lines. Distribute reports and data to internal and external third parties according to applicable regulations, standard operating procedures (SOPs), and internal guidelines, with guidance and support from senior operation team members. Fluency in English and Spanish is required.
Responsibilities
- Process safety data according to applicable regulations, guidelines, SOPs, and project requirements.
- Perform pharmacovigilance activities, including collecting and tracking incoming adverse events (AEs) and endpoint information; determining the initial or update status of incoming events; database entry; coding AEs and products; writing narratives; and literature-related activities.
- Meet quality, productivity, and delivery standards according to project requirements.
- Liaise with functional team members and healthcare professionals to address project-related issues.
Requirements
- Bachelor’s degree in life sciences or a related field (mandatory).
- Fluency in English and Spanish (mandatory; will be evaluated).
- Pharmacovigilance experience is highly valued (desirable).
- Experience with safety databases, including ARGUS or others, is highly valued (desirable).
- Work modality: 100% home-based.
Datos clave
- Work modality: 100% home-based.
- A bachelor’s degree in life sciences or a related field is mandatory.
- Fluency in English and Spanish is mandatory and will be evaluated.
- Pharmacovigilance and safety database experience are desirable.
Preguntas frecuentes
What does the Operations Specialist 1 role involve?
The role reviews, assesses, and processes safety data and information, and distributes reports and data according to applicable regulations, SOPs, and internal guidelines.
What qualifications are required?
A bachelor’s degree in life sciences or a related field and fluency in English and Spanish are mandatory. Pharmacovigilance and safety database experience are desirable.
What pharmacovigilance activities are included?
Activities include collecting and tracking adverse events and endpoint information, database entry, coding, writing narratives, and literature-related work.