どんな仕事かAIによる生成

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. The role involves collecting and reviewing adverse event reports, conducting initial assessment and coding, preparing and submitting expedited safety reports, and maintaining safety databases and tracking systems. You will collaborate with cross-functional teams to support timely and accurate safety data reporting.

応募資格・募集要項・仕事内容を見る

応募資格

必須

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%)

応募について

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.

募集要項最終確認 11/8

職種: 臨床開発・薬事
雇用形態: Permanent
給与: 記載なし
給与の詳細: In addition to your competitive salary, ICON offers a range of additional benefits.
勤務地: 東京都Tokyo大阪府Osaka
働き方: Drug Safety Associate - Tokyo Osaka - Office Hybrid
休日・休暇: Various annual leave entitlements
福利厚生: 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, LifeWorks, 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 assuranceFlexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.
経験年数: 1年以上
学歴: 大学卒業以上
応募締切: 2027/08/19
掲載日: 2026/10/13 02:35（28日前）
最終確認: 2026/11/08 22:16（2日前）

仕事内容

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.

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職種と勤務地が似ている求人東京都の臨床開発・薬事 240件

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Drug Safety Associate

どんな仕事かAIによる生成

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応募資格

必須

応募について

募集要項最終確認 11/8

仕事内容

What You Will Do:

同じ会社の求人12件

職種と勤務地が似ている求人東京都の臨床開発・薬事 240件

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