Pharmacovigilance Reporting Specialist — Hybrid

KCR Placement; Ciudad de México; Hybrid; MXN 600,000 - 750,000; Full time

Job summary

ICON is a global healthcare intelligence and clinical research organization driving faster access to medicines. We are seeking a Pharmacovigilance Reporting Associate (Intelligence) to accurately prepare safety reports for clinical trials and post-marketing activities, while leading safety reporting intelligence projects as needed.

You will work within a collaborative, hybrid-environment, upholding ICON's values and ensuring regulatory and client requirements are met with precision and

Qualifications

• Bachelor's degree in life sciences, pharmacy, or related field.
• Experience in pharmacovigilance or drug safety preferred.
• Strong attention to detail and organizational skills.

Responsibilities

• Prepare safety reports accurately and on time for trials and post-marketing activities.
• Serve as safety reporting intelligence processor or lead on projects.
• Adhere to SOPs, regulatory requirements, and client processes.
• Demonstrate client management, scope, submission compliance, quality, and budget focus.
• Collaborate within a multidisciplinary team in a fast-paced, regulated environment.
• Support process improvements and value-driven business outcomes.

Skills

Pharmacovigilance

Safety reporting

Regulatory compliance

Education

Bachelor's degree in life sciences/pharmacy

Job description

ICON is a global healthcare intelligence and clinical research organization driving faster access to medicines. We are seeking a Pharmacovigilance Reporting Associate (Intelligence) to accurately prepare safety reports for clinical trials and post-marketing activities, while leading safety reporting intelligence projects as needed.

You will work within a collaborative, hybrid-environment, upholding ICON's values and ensuring regulatory and client requirements are met with precision and