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MEX - Pharmacovigilance Reporting (Associate & Senior Associate)

ICON plc

Ciudad de México

Presencial

MXN 300,000 - 600,000

Jornada completa

Hace 30+ días

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Descripción de la vacante

An established industry player is seeking a Pharmacovigilance Reporting Associate/Senior Associate to join their dynamic team. In this role, you will be instrumental in preparing and reviewing safety reports related to clinical trials and post-marketing activities, ensuring compliance with regulatory standards. You will collaborate with cross-functional teams to manage safety data effectively, contributing to patient safety and regulatory compliance. This is an exciting opportunity to work in a supportive environment that values diversity and innovation, offering competitive benefits and a commitment to your professional growth.

Servicios

Various annual leave entitlements
Health insurance offerings
Competitive retirement planning
Global Employee Assistance Programme
Life assurance
Flexible optional benefits

Formación

  • Bachelor's degree in life sciences or pharmacy required.
  • Experience in pharmacovigilance or drug safety is essential.

Responsabilidades

  • Prepare and review safety reports ensuring accuracy and compliance.
  • Analyze adverse event data from clinical trials for safety reports.

Conocimientos

Pharmacovigilance
Attention to Detail
Communication Skills
Organizational Skills
Project Leadership

Educación

Bachelor's degree in life sciences
Bachelor's degree in pharmacy

Descripción del empleo

MEX - Pharmacovigilance Reporting (Associate & Senior Associate)

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.

We are currently seeking a Pharmacovigilance Reporting Associate/Senior Associate (Leader role) to join our diverse and dynamic team!

Location: Mexico City (office-based an average of 3 days per week)

As a Pharmacovigilance Reporting Associate/Senior Associate (Leader role) at ICON, you will be responsible for the accurate and timely preparation of safety reports related to clinical trials and post-marketing activities. You will ensure compliance with regulatory requirements and contribute to the effective management of safety data to support patient safety and regulatory compliance.

What You Will Be Doing:

  • Preparing and reviewing safety reports, including periodic safety updates and individual case safety reports, ensuring accuracy and compliance with regulatory standards.
  • Collecting and analyzing adverse event data from clinical trials and post-marketing sources to support the preparation of comprehensive safety reports.
  • Maintaining up-to-date knowledge of regulatory requirements and industry best practices related to pharmacovigilance reporting.
  • Collaborating with cross-functional teams, including clinical, regulatory, and data management, to gather necessary information and resolve any reporting issues.
  • Ensuring the timely submission of safety reports to regulatory authorities and sponsors, adhering to established deadlines and guidelines.

Your Profile to be Associate:

  • Bachelor’s degree in life sciences, pharmacy, or a related field.
  • Experience in pharmacovigilance or drug safety, with a strong understanding of safety reporting processes and regulatory requirements.
  • Excellent attention to detail and organizational skills, with the ability to prepare and review complex safety reports accurately.
  • Strong communication and collaboration skills, with experience working effectively within a multidisciplinary team.
  • Ability to manage multiple tasks and prioritize effectively in a fast-paced, regulated environment.

Your Profile to be Senior Associate:

  • Bachelor’s degree in life sciences, pharmacy, or a related field.
  • Experience in pharmacovigilance or drug safety, with a strong understanding of safety reporting processes and regulatory requirements.
  • Experience leading projects or studies
  • Excellent attention to detail and organizational skills, with the ability to prepare and review complex safety reports accurately.
  • Strong communication and collaboration skills, with experience working effectively within a multidisciplinary team.
  • Ability to manage multiple tasks and prioritize effectively in a fast-paced, regulated environment.

What ICON can offer you:

Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.

In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work-life balance opportunities for you and your family.

Our benefits examples include:

  • Various annual leave entitlements
  • A range of health insurance offerings to suit you and your family’s needs.
  • Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
  • Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being.
  • Life assurance
  • Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.

At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here.

Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.

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

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