Pharmacovigilance Specialist
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 Reporting Specialist at ICON, you will be responsible for the timely and accurate preparation of pharmacovigilance reports, ensuring compliance with regulatory requirements and internal policies.
What You Will Do:
You will contribute to pharmacovigilance and drug safety activities, taking responsibility for your deliverables and working collaboratively.
Key responsibilities include:
Preparing and submitting comprehensive safety reports, including periodic safety update reports (PSURs) and individual case safety reports (ICSRs), in compliance with regulatory standards.
Conducting thorough data analysis to identify trends and assess the safety profile of pharmaceutical products.
Collaborating with cross-functional teams to ensure timely and accurate reporting of adverse events.
Maintaining up-to-date knowledge of pharmacovigilance regulations and industry best practices to ensure compliance.
Providing training and support to team members on pharmacovigilance reporting processes and requirements.
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
Significant experience in pharmacovigilance reporting or drug safety within a clinical or pharmaceutical environment.
Strong analytical skills with proficiency in data analysis tools and reporting software.
Excellent communication and interpersonal skills, facilitating effective collaboration with internal and external stakeholders.
A commitment to maintaining high standards of quality and compliance in all pharmacovigilance activities.
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 Reporting Specialist at ICON, you will be responsible for the timely and accurate preparation of pharmacovigilance reports, ensuring compliance with regulatory requirements and internal policies.
What You Will Do:
You will contribute to pharmacovigilance and drug safety activities, taking responsibility for your deliverables and working collaboratively.
Key responsibilities include:
Preparing and submitting comprehensive safety reports, including periodic safety update reports (PSURs) and individual case safety reports (ICSRs), in compliance with regulatory standards.
Conducting thorough data analysis to identify trends and assess the safety profile of pharmaceutical products.
Collaborating with cross-functional teams to ensure timely and accurate reporting of adverse events.
Maintaining up-to-date knowledge of pharmacovigilance regulations and industry best practices to ensure compliance.
Providing training and support to team members on pharmacovigilance reporting processes and requirements.
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
Significant experience in pharmacovigilance reporting or drug safety within a clinical or pharmaceutical environment.
Strong analytical skills with proficiency in data analysis tools and reporting software.
Excellent communication and interpersonal skills, facilitating effective collaboration with internal and external stakeholders.
A commitment to maintaining high standards of quality and compliance in all pharmacovigilance activities.
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