ICON

Drug Safety Associate

Japan · Work style not stated · Full time

Apply on the employer’s site ↗See how well you match this job

You apply directly with the employer. ROLIVA does not submit applications from this page and is not the employer.

About the role

Description from the employer’s posting. Check the employer’s page for the current version.

  • EmployerICON
  • LocationJapan
  • Work styleWork style not stated
  • Employment typeFull time
  • Employer posted

Drug Safety Associate - Tokyo Osaka - Office Hybrid

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 Drug Safety Associate at ICON, you will ensure the safety of investigational drugs and contribute to the advancement of innovative treatments and therapies.

What You Will Do:

Your role will involve delivering pharmacovigilance and drug safety work to a high standard, working closely with your team and stakeholders.

Key responsibilities include:

  • 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.
Show full description

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 a scientific or healthcare-related field.
  • 1-2 years of experience in pharmacovigilance or drug safety within the pharmaceutical or biotechnology industry preferred.
  • Knowledge of pharmacovigilance regulations and guidelines (e.g., ICH, FDA, EMA).
  • Strong attention to detail and ability to work effectively in a fast-paced environment.
  • Excellent communication and organizational skills, with the ability to collaborate across teams and prioritize tasks efficiently.
  • Willingness to travel as required (approximately 10%)

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

Staying safe while you apply

  • Never pay to apply, interview or accept an offer. ROLIVA never asks you for payment to apply to a job.
  • Apply only through the official “Apply on the employer’s site” button, on the employer’s own site, and check that a recruiter’s email uses that employer’s own domain rather than a free email address.
  • Be cautious of an offer made with no real interview, or pressure to decide quickly or share financial details early.

Does something look wrong with this listing? Use “Report broken link” in the role details, or read ROLIVA’s full job-safety guidance ↗.

Preparing for this role with ROLIVA

  • Check the fit.

    Compare the requirements with the experience you have confirmed, including gaps.

  • Prepare honestly.

    Build interview stories and application drafts from your own evidence.

  • Keep track.

    Save the role and record your own application status and follow-ups.

Create a free workspace or log in.

At a glance

  • Employment typeFull time
  • SeniorityEntry level
  • Employer posted
  • Added to ROLIVA
  • Last checked

Explore similar roles

Similar jobs

ICON

Oracle DBA III

India

Work style not statedFull time

ICON

CRA 3

Australia

Remote (restrictions not stated)Full time