I

Icon

Global drug and device development services

Drug Safety Associate

Clinical Research OperationsConfirmed live in the last 24 hours
Full-timeNo salary listed

About the Job

Requirements

  • A bachelor's degree in a scientific or healthcare-related field is required.
  • Knowledge of pharmacovigilance regulations and guidelines, including ICH, FDA, and EMA, is required.
  • Willingness to travel approximately 10% as required.

Responsibilities

  • Collect and review adverse event reports from clinical trials and post-marketing sources.
  • Conduct initial assessment and coding of adverse events according to established procedures and regulatory guidelines.
  • Prepare and submit expedited safety reports to regulatory authorities and investigators as required.
  • Assist in the development and maintenance of safety databases and tracking systems.
  • Collaborate with cross-functional teams to ensure timely and accurate reporting of safety data.

Desired Qualifications

  • 1–2 years of experience in pharmacovigilance or drug safety within the pharmaceutical or biotechnology industry is preferred.

About the Company

Icon

Global drug and device development services

This company provides consulting, development, and commercialization support for drugs and medical devices through a global network of offices. Its team across 53 countries offers end-to-end services, from strategy and regulatory work to manufacturing and market access, helping clients shorten development time, lower costs, and raise quality. It differentiates itself with wide geographic reach and a clear focus on reducing time to market and cost while leveraging deep experience across many therapeutic areas. Its goal is to help clients accelerate the development of life-saving products and improve quality of life by delivering reliable information, practical solutions, and solid performance.

Company size
10,001+
Company stage
IPO
Headquarters
Ireland
Founded
1990

Recently Posted Jobs

Explore more opportunities at Icon

See more jobs