Hiring.Camp

Pharmacovigilance Assistant II

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Yesterday

Location
Poland, Warsaw · Bulgaria, Sofia
Workplace
Onsite
Type
Full-time
Education
Bachelor
Visa
Not sponsored
Source
Workday

Description

Pharmacovigilance Assistant II

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 Assistant II at ICON, you will ensure the accurate collection, processing, and reporting of safety data for clinical trials and marketed products.


What You Will Do:

You will take responsibility for pharmacovigilance and drug safety deliverables, applying your skills to ensure quality and efficiency.

Key responsibilities include:

  • Overseeing the collection, processing, and timely reporting of adverse event reports in compliance with regulatory requirements.
  • Ensuring accurate data entry and maintenance of pharmacovigilance databases, reviewing reports for consistency and completeness.
  • Assisting in the preparation of periodic safety reports, including risk-benefit analyses, for regulatory submissions and sponsors.
  • Collaborating with internal teams and external stakeholders to resolve queries related to safety data and pharmacovigilance activities.
  • Supporting audit and inspection readiness by maintaining comprehensive documentation of pharmacovigilance activities and safety reports.

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 life sciences, pharmacy, or a related field.
  • Previous experience in pharmacovigilance or drug safety, with a solid understanding of regulatory requirements and safety reporting processes.
  • Excellent attention to detail and strong organizational skills, with the ability to manage complex data sets and reports.
  • Strong communication and teamwork skills, with experience collaborating across cross-functional teams and external partners.
  • Ability to work in a fast-paced environment, ensuring compliance with regulatory guidelines and timelines.

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

Skills

Clinical TrialsCompliance