Pharmacovigilance Safety Analyst (Bilingual EN/ES)

IQVIA; Estado de México; Presencial; MXN 350.000 - 550.000; Jornada completa

Descripción de la vacante

IQVIA, a leading global provider of clinical research services, is seeking a Pharmacovigilance professional to review, assess, and process safety data across service lines in Mexico. You will work under the guidance of senior operations staff to ensure compliant reporting and data distribution to internal and external stakeholders.

Responsibilities include processing events, coding, narratives, literature activities, and maintaining data integrity while meeting quality and productivity targets.

Formación

• Bachelor’s degree in Life sciences or related field.
• Fluency in English and Spanish.
• 1–2 years pharmacovigilance experience (desirable).
• Experience with Safety Databases (ARGUS or others) (desirable).
• Knowledge of global, regional, local regulatory requirements.
• Attention to detail and accuracy.
• MS Office and web-based applications knowledge.
• Strong organizational and time management skills.
• Strong verbal/written communication skills.

Responsabilidades

• Prioritize and complete trainings on time.
• Process Safety data according to regulations, guidelines, SOPs and project requirements.
• Perform Pharmacovigilance activities including collecting adverse events/endpoints.
• Database entry.
• Code AE and products, write narratives, literature activities.
• Meet quality and productivity standards.
• Create, maintain and track cases per project plan.
• Identify quality problems and escalate to senior team member.
• Mentor new team members if assigned by the Manager.
• Attend project team meetings and provide feedback on challenges/successes.
• Ensure 100% compliance with people practices and processes.
• Perform other duties as assigned.

Conocimientos

Attention to detail

Time management

Communication skills

Self-motivation

Educación

Bachelor’s degree in Life sciences

Herramientas

Microsoft Office

Descripción del empleo

IQVIA, a leading global provider of clinical research services, is seeking a Pharmacovigilance professional to review, assess, and process safety data across service lines in Mexico. You will work under the guidance of senior operations staff to ensure compliant reporting and data distribution to internal and external stakeholders.

Responsibilities include processing events, coding, narratives, literature activities, and maintaining data integrity while meeting quality and productivity targets.