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Location
Remote (Mexico)
Employment
Full-Time

Confirmed on the employer's own hiring board on Nov 6, 2026. First seen by Alion on Nov 4, 2026. ICON scores A on the Alion truth index.

Overview
Company
Impact
Profile match
ICON is an Irish clinical research organisation that provides outsourced clinical development and commercialisation services to pharmaceutical, biotechnology and medical device companies, from early-phase trials to late-stage studies, laboratory services and real-world evidence. Founded in 1990 and listed on Nasdaq, it operates worldwide with tens of thousands of employees. The company is headquartered in Dublin, Ireland.
Home Based - CDMX - Exp. People Lead

At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise.

As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide.

As a Supervisor, Pharmacovigilance at ICON, you will oversee the safety monitoring and reporting of adverse events related to clinical trials and marketed products.

What You Will Do:

You will manage day-to-day pharmacovigilance and drug safety activities, supporting your team to deliver quality outcomes.

Key responsibilities include:

  • Supervising the day-to-day pharmacovigilance operations, ensuring timely and accurate reporting of adverse events.
  • Collaborating with cross-functional teams, including clinical operations and regulatory affairs, to optimize pharmacovigilance processes.
  • Ensuring compliance with global regulatory requirements and internal standard operating procedures for safety reporting.
  • Managing safety data collection, analysis, and submission to regulatory authorities.
  • Providing leadership and training to the pharmacovigilance team, ensuring adherence to best practices in safety monitoring.

Your Profile:

You will have solid pharmacovigilance and drug safety experience, with the ability to manage competing priorities and develop your team.

Required qualifications and experience:

  • Bachelor's degree in life sciences, pharmacy, or a related field.
  • Experience in pharmacovigilance or drug safety, with a focus on clinical trials or post-marketing surveillance.
  • Strong knowledge of global pharmacovigilance regulations and guidelines.
  • Excellent communication, leadership, and organizational skills, with the ability to manage a team effectively.
  • Detail-oriented with the ability to manage multiple tasks and ensure accuracy in safety reporting.

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

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