Pharmacovigilance Associate
Home Based - CDMX
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
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.
Excellent communication and interpersonal skills, enabling effective collaboration with team members and stakeholders.
A commitment to maintaining high standards of quality and compliance in all pharmacovigilance activities.
Willingness to travel as required (approximately 10%)
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
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
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.
Excellent communication and interpersonal skills, enabling effective collaboration with team members and stakeholders.
A commitment to maintaining high standards of quality and compliance in all pharmacovigilance activities.
Willingness to travel as required (approximately 10%)
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