See what comes ahead in the application process. Find out how we help you land that job.
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apply with randstad.
Applying with us is easy. We will review your application and see if you are a good fit for the job and the company.
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we'll give you a call.
Our consultant will call you at a suitable time to discuss your application and further career aspirations.
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getting you registered.
If you’ve never worked with us before, we’ll need some basic additional pieces of information to confirm your eligibility for work.
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compliance check.
Next, we just need to verify a few things - we’ll make the relevant compliance checks and keep you posted.
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reference and background check.
As part of the process in ensuring you’re perfect for the role, we’ll make contact with any relevant references you’ve provided.
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the perfect job for you.
Our expert team will either arrange an interview for the role you’ve applied for, or if they believe there’s a better opportunity, they’ll suggest alternative options too.
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the interview.
We’ll ensure that you’re fully prepared ahead of your interview and know exactly what to expect - good luck!
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start your new job.
Congratulations, you’re ready to begin your new job. The team will ensure that you’re fully prepared for your first day.
¥10,000,000 - ¥12,000,000 per year, 年収1,000 ~ 1,200万円
社名社名非公開職種研究、非臨床業務内容ニューロサイエンス領域あるいは感染症領域における創薬研究の牽引.複数の専門部署や国内外の協業パートナーと連携し,チームメンバーを率いて創薬研究を推進. Lead drug discovery research in the field of neuroscience or infectious diseases. Leading drug discovery research by collaborating with multiple specialized departments and domestic and international collaborating partners.求められる経験【必須要件(Essential criteria)】ニューロサイエンス領域あるいは感染症領域における薬理研究実績があることMust have a proven track record of pharmacological research in the neurosc
社名社名非公開職種研究、非臨床業務内容ニューロサイエンス領域あるいは感染症領域における創薬研究の牽引.複数の専門部署や国内外の協業パートナーと連携し,チームメンバーを率いて創薬研究を推進. Lead drug discovery research in the field of neuroscience or infectious diseases. Leading drug discovery research by collaborating with multiple specialized departments and domestic and international collaborating partners.求められる経験【必須要件(Essential criteria)】ニューロサイエンス領域あるいは感染症領域における薬理研究実績があることMust have a proven track record of pharmacological research in the neurosc
¥7,000,000 - ¥12,000,000 per year, 年収700 ~ 1,200万円
社名社名非公開職種薬事、メディカルライティング業務内容バイオ医薬品、ワクチン及び低分子医薬品の開発段階から承認維持管理に関するCMC薬事戦略立案,資料作成,当局対応等の業務全般を担当する. Responsible for all aspects of CMC regulatory strategy development, documentation creation, regulatory agency interactions, and maintenance management from the development stage to approval for biopharmaceuticals, vaccines, and small molecule drugs.求められる経験【必須要件】・製薬企業でのバイオ医薬品又は低分子医薬品のCMC薬事又はCMC関係の業務経験7年以上または行政官として品質に関する審査経験5年以上・英語・日本語でのコミュニケーション能力【望ましい要件】・CMC薬事担当者
社名社名非公開職種薬事、メディカルライティング業務内容バイオ医薬品、ワクチン及び低分子医薬品の開発段階から承認維持管理に関するCMC薬事戦略立案,資料作成,当局対応等の業務全般を担当する. Responsible for all aspects of CMC regulatory strategy development, documentation creation, regulatory agency interactions, and maintenance management from the development stage to approval for biopharmaceuticals, vaccines, and small molecule drugs.求められる経験【必須要件】・製薬企業でのバイオ医薬品又は低分子医薬品のCMC薬事又はCMC関係の業務経験7年以上または行政官として品質に関する審査経験5年以上・英語・日本語でのコミュニケーション能力【望ましい要件】・CMC薬事担当者