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Senior Specialist, Medical Affairs
年収：800万 ～ 1200万
採用企業案件
オルガノン株式会社
-
- 資本金100百万円
- 会社規模非公開
- 医薬品メーカー
- 医薬品卸
| 部署・役職名 | Senior Specialist, Medical Affairs |
|---|---|
| 職種 | |
| 業種 | |
| 勤務地 | |
| 仕事内容 |
The Position The primary responsibilities of the Medical Services, Sr. Specialist is to triage and respond to all inquiries received through different channels from healthcare providers and other external stakeholders, and manage the processes related to promotional review ensuring the highest standards in medical communications. Responsibilities: * Medical Information ・Respond to or triage unsolicited on-label and off-label inquiries received from healthcare providers and other external and internal stakeholders. ・Ensure that responses to medical inquiries are high-quality professional communications. ・Set-up standardized answers for frequently asked questions or routine requests, in collaboration with Medical Advisors and Medical Science Liaisons. ・Research, assess, and compile responses from published and unpublished literature to create clinical support in a fair, balanced, and scientifically accurate format. ・Report adverse events and product quality complaints to the appropriate departments. * DPOC (Designated Point of Contact) Process Management ・Ensure receipt, classification, and appropriate routing of product inquiries for further processing to meet regulatory and business requirements. ・Assure DPOC database is accurately maintained. ・Generate and report DPOC monthly key performance metrics. ・Identify gaps within the medical information process and provide rapid resolution. ・Support and train Medical Advisors/Medical Science Liaison and other staff in the management of DPOC/medical information requests. * Medical Review ・Manage all the processes related to promotional material review and approval (i.e. review flows, priorities, outsourcing, metrics, SOP, implementation of regional initiatives). ・Be knowledgeable of the different regulations and laws governing promotional materials in the country. ・Ensure that medical review of materials is completed with accuracy and in a timely manner, meeting company policies and country regulations prior to public release. ・Provide compliance leadership and training to country staff. |
| 労働条件 |
契約社員（1 year contractor） |
| 応募資格 |
【必須（MUST）】 Required Experience and Skills:・Minimum of 3 years of pharmaceutical experience ( Experience in medical information, contact center, medical review, or other related field preferred, but other role (including MR ) may be considered). ・Experience of women's health related products. ・High level of scientific and ethical integrity. Strong sense of responsibility for the response deadlines ・Excellent communication and collaboration skills. ・Understanding of domestic regulations and industry codes ・Understanding of core systems, tools, and metrics related to medical literature. ・English: Business level |
| アピールポイント | マネジメント業務なし フレックスタイム |
| リモートワーク | 可 「可」と表示されている場合でも、「在宅に限る」「一定期間のみ」など、条件は求人によって異なります |
| 受動喫煙対策 | 屋内禁煙 |
| 更新日 | 2024/11/14 |
| 求人番号 | 4033923 |
採用企業情報
- オルガノン株式会社
-
- 資本金100百万円
- 会社規模非公開
- 医薬品メーカー
- 医薬品卸
-
会社概要
【設立年月日】2020年3月31日
【代表者】櫻井 亮太
【資本金】1億円
【本社所在地】東京都港区南青山1-24-3
【事業内容】医療用医薬品輸入製造販売
転職・求人情報の詳細をご覧になる場合は会員登録（無料）が必要です