Pharmacovigilance Associate

ICR United States USA

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Brazil, Sao Paulo Until 10/3/2026 1+ years exp First posted August 4, 2026 Last posted August 4, 2026
Job description
Pharmacovigilance Associate

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.


As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.


As a Pharmacovigilance Associate at ICON, you will monitor and ensure the safety of pharmaceutical products by collecting, analyzing, and reporting adverse event information.

What You Will Do:

Your role will involve delivering pharmacovigilance and drug safety work to a high standard, working closely with your team and stakeholders.

Key responsibilities include:

  • Collecting and reviewing adverse event reports to ensure accurate and timely reporting in accordance with regulatory guidelines.
  • Conducting signal detection and risk assessment activities to identify potential safety issues.
  • Collaborating with cross-functional teams to support safety-related inquiries and investigations.
  • Maintaining up-to-date knowledge of pharmacovigilance regulations and industry best practices.
  • Assisting in the preparation of safety reports and regulatory submissions.

Your Profile:

You will bring relevant pharmacovigilance and drug safety experience, along with the following qualifications and skills.

Required qualifications and experience:

  • Bachelor's degree in a relevant scientific discipline or healthcare-related field
  • 1 year of experience in pharmacovigilance, drug safety, or a related area, preferably within a clinical or pharmaceutical environment.
  • Strong analytical skills with attention to detail in data collection and reporting.
  • A commitment to maintaining high standards of quality and compliance in all pharmacovigilance activities.
  • Based in Sao Paulo - Remote position
  • Intermediate level of English

Employment with ICON is contingent upon having the legal right to work in the country where the role is based.


Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.


Benefits may include:

  • Competitive base salary and performance related incentives
  • Health and wellbeing programmes including medical, dental, and vision coverage where applicable
  • Retirement and pension plans
  • Life assurance and disability coverage
  • Employee assistance programmes and wellbeing resources
  • Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.


Visit our careers site to read more about the benefits ICON offers.


Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.


If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.

Are you a current ICON Employee? Please click here to apply

About this role

Summary

Monitor, analyze, and report adverse events to ensure drug safety and compliance.

Job title

Pharmacovigilance Associate

Experience level

1 year of experience

Minimum experience

1+ years exp

Industry

healthcare

Location requirements

Remote position in Sao Paulo, Brazil.

Salary

Not specified

Management role

No

Skills & keywords

Required skills

data collectionreportingregulatory knowledgeanalytical skills

Preferred skills

None specified

Specializations

pharmacovigilancedrug safety
Locations

Structured locations inferred from the posting.

Brazil

Remote Country

São Paulo, State of São Paulo, Brazil

On-site City