Regulatory and product development consulting • early phase clinical research • phase II-III clinical research • late phase clinical research • eClinical solutions
10,000+ employees
Founded 1983
⚕️ Healthcare Insurance
🧬 Biotechnology
💊 Pharmaceuticals
💰 Venture Round on 1990-01
December 3
Regulatory and product development consulting • early phase clinical research • phase II-III clinical research • late phase clinical research • eClinical solutions
10,000+ employees
Founded 1983
⚕️ Healthcare Insurance
🧬 Biotechnology
💊 Pharmaceuticals
💰 Venture Round on 1990-01
•Review NDA/ CDAs, Statement of oath to sites, Advisory agreement, termination agreement, marketing materials or other basic legal documents under the supervision of Assistant General Counsel (Japan) •Organize and file legal documents, such as signed agreements and templates, and provide templates to internal stakeholders •Keep and handle corporate stamps under the supervision of Assistant General Counsel (Japan) •Prepare and draft minutes of shareholders meeting/directors meeting, file for registration in the corporate register in Legal Affairs Bureau, translate minutes into English and keep the record. •Prepare agenda and minutes of the monthly local Compliance Committee as a secretary which discuss compliance issues •Conduct basic legal research or collect necessary data/fact to be used •Provide administrative support such as KOFAX system and law firm invoices management
•法律事務所 パラリーガル、アシスタント業務経験 •法務部門 アシスタント業務 •コンサルティング企業 契約関連業務アシスタント業務経験 • 英語読み書き(TOEIC600目安)
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