Jobs Companies ICON plc Pharmacovigilance Assistant I

À propos de ce poste Pharmacovigilance Assistant I chez ICON plc

ICON plc · Hybride · Brazil, Sao Paulo
Pharmacovigilance Assistant I

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.


We are currently seeking a Pharmacovigilance Assistant I to join our diverse and dynamic team. As a Pharmacovigilance Assistant I at ICON, you will play a key role in supporting the collection, documentation, and reporting of safety data related to medications and clinical trials. You will help ensure compliance with regulatory requirements, contributing to patient safety and the ongoing success of clinical research programs.

Locations:

- Mexico City (MEXICO)

- São Paulo (BRAZIL)

Contract Type:

- Permanent

- Hybrid work model (3 days per week in the office and 2 days working from home)

What You Will Be Doing:

  • Supporting the collection, review, and processing of adverse event reports related to clinical trials and marketed products.

  • Ensuring timely and accurate data entry of safety information into pharmacovigilance databases.

  • Assisting in the preparation and submission of safety reports to regulatory authorities and sponsors, as required.

  • Collaborating with cross-functional teams to maintain compliance with safety regulations and company protocols.

  • Maintaining detailed records and documentation related to pharmacovigilance activities and safety reporting.

Your Profile:

  • Basic understanding of pharmacovigilance principles and regulatory requirements is preferred.

  • Strong attention to detail and organizational skills, with the ability to manage multiple tasks efficiently.

  • Effective communication and collaboration skills, with a focus on maintaining accuracy in documentation and reporting.

  • Ability to work in a fast-paced, regulated environment, ensuring compliance with safety guidelines and protocols.

#LI-FP1

#LI-Hybrid


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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À propos de ICON plc

ICON is an award-winning workplace that enables you to make a difference to patients’ lives by being part of a world-class clinical research organisation that helps deliver new medicines & medical devices that are benefitting patients worldwide. You are also part of a diverse company that cares about our world and is dedicated to conducting business more sustainably and supporting the communities in which we live. If you’re as driven as we are, join us. You’ll be working in a great environment, with some of the brightest and the friendliest people in the sector, and you’ll be helping shape an industry.

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