Safety Manager
募集要項
| JoB No. | 376 |
|---|---|
| 業種 | CRO/SMO/CSO |
| ポジション名 | Safety Manager |
| 職種 | PMS/PV |
| 業務内容 |
• Provide Safety advices for documents submitting to Regulatory authorities. • Provide Safety related expertise for answering queries from Regulatory authorities, sites and institutional review boards. • Review of adverse events and serious adverse events, laboratory data review and coding data review. • Manage start-up of new projects using standard operating procedures and best practices, including identifying potential risks during project initiation and implementing mitigation measures to ensure seamless delivery at maintenance stage. • Collaborating with project study teams, provide training and mentoring to team members to improve skill levels and productivity • Develop customer relationships into partnerships; manage accounts targeting extended business relationship throughout lifecycle. Focus on customer loyalty and contract renewal. • Prepare quotations for bidding projects and supports to preparation of bid defense materials. • Perform other duties assigned by the CEO and Vice President, Clinical Development |
| 勤務地 | 東京都 |
| 応募資格 |
• Bachelor’s degree of health science or other related fields. • 4 years’ experience of Pharmacovigilance (CEVA, Medical Information, Safety Publishing, Risk Management etc.) and 2 years’ project management experience in in Contract Research Organizations or Pharmaceutical companies • Strong project management; planning and organizational skills – Ability to deliver on multiple projects and manage competing priorities. – Independent judgment, negotiating, decision-making, and problem-solving skills. • Business-level proficiency of English and Japanese |
| 雇用形態 | 正社員/契約社員 |
| 年収目安 | 想定年収：600万～850万 |
| 備考 | －－－ |
| 担当コンサルタント | 小川 善之 |
企業情報
| 企業名 | — |
|---|---|
| 事業内容・会社の特徴 | — |
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