Pharmacovigilance Safety Reporting Specialist (Hybrid)

ICON Clinical Research; Ciudad de México; Híbrido; MXN 360.000 - 540.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Annual leave entitlements

Health insurance

Retirement planning

Global Employee Assistance Programme

Life assurance

Descripción de la vacante

ICON Clinical Research is seeking a Pharmacovigilance Reporting Associate (Intelligence) to prepare safety reports for clinical trials and post‑marketing activities. You will operate as a safety reporting intelligence processor or lead, ensuring timely submissions and compliance while aligning with ICON values of people, clients and performance.

The role emphasizes collaboration within multidisciplinary teams, adherence to SOPs, and a focus on process improvement to streamline workflows and add

Formación

• Experience in pharmacovigilance or drug safety with an understanding of safety reporting processes and regulatory requirements.
• Excellent attention to detail and organizational skills.
• Strong communication and collaboration abilities in a multidisciplinary team.
• Ability to manage multiple tasks in a fast-paced, regulated environment.

Responsabilidades

• Serve as safety reporting intelligence processor and lead on multiple projects.
• Adhere to ICON values centering on People, Clients and Performance.
• Contribute to process improvements to streamline workflows and add value.
• Complete departmental project activities accurately per ICON SOPs and procedures.
• Handle safety reporting activities with a customer-focused mindset and audit readiness.
• Demonstrate skills in client management, safety reporting, project scope, submission compliance, quality and budgeting.

Conocimientos

Pharmacovigilance

Attention to detail

Communication

Multitasking

Team collaboration

Educación

Bachelor's degree in life sciences, pharmacy, or a related field

Descripción del empleo

ICON Clinical Research is seeking a Pharmacovigilance Reporting Associate (Intelligence) to prepare safety reports for clinical trials and post‑marketing activities. You will operate as a safety reporting intelligence processor or lead, ensuring timely submissions and compliance while aligning with ICON values of people, clients and performance.

The role emphasizes collaboration within multidisciplinary teams, adherence to SOPs, and a focus on process improvement to streamline workflows and add