- 常勤
- 東京都
【東京都新宿区】大手外資系製薬メーカーの求人です
Medical Manager, Immunology Pipeline Medical 週5日1000万円～
- 300411520
- 2024年08月22日更新
- 当直なし
- オンコールなし
| 勤務地 | 東京都新宿区 |
|---|---|
| 給与（年収） | 1000万円 応相談 |
| 募集科目 | 呼吸器内科、消化器内科、リウマチ内科、皮膚科、製薬会社 |
| 交通アクセス | *** |
| 医療機関区分 | その他会社 |
| 病床数 | ・・・ |
| 屋内の受動喫煙対策 | 敷地内禁煙 |
求人情報
勤務内容・条件
| 募集科目 | 呼吸器内科、消化器内科、リウマチ内科、皮膚科、製薬会社 |
|---|---|
| 勤務内容 | その他 Responsible for planning and executing medical activities and make sure timely and effective execution aligned to medical strategy. 1. Key accountabilities 1-1. Lead Medical Strategy ■ Lead and monitor the execution of the Japan Medical Plan to ensure on-time and on-budget delivery of all tactical activities or deliverables ■ Provide medical and technical input into medically accurate development of Brand promotional materials in close alignment with marketing team and communicate the details and progress of the Medical Plan to local Medical Team, the Global Medical and all parties responsible for execution ■ Work with cross-functional, multidisciplinary teams to facilitate the creation of medical strategies about products to answer unsolicited medical requests from internal and external stakeholders and ensure strategic and cross-functional alignment across the organization and any joint ventures to achieve the medical mission of supporting safe and appropriate use of a particular brand(s)/ projects ■ Leverage (unmet) medical needs in order to support lifecycle opportunities based on patient needs on a rolling basis through the development cycle 1-2. Evidence generation ■ Liaise with key internal stakeholders to help develop, secure approval for and implement independent post approval studies that have the potential to support Sanofi products. Review, approve and supervise all aspects of clinical study programs, including preparation of study protocols, case report forms, study reports, statistical analysis plans, clinical trial guidelines and the accurate and timely reporting of study data ■ Oversee conduct of all clinical studies in adherence to both Company standards, and government/industry regulations (GCP/ICH) ■ Actively engage regional thought leaders, investigators and potential investigators in two-way scientific communication around ISS/phase IV studies ■ Lead the review and approval of the concepts/protocols of Post-Authorization Safety/Effectiveness Studies (PASS/PAES), Investigator Sponsored Study (ISS) and Diagnostic Testing Programs, according to applicable SOP(s) ■ Advise on locally driven early stage clinical trial plans ■ Maintain up-to-date working knowledge and adherence of all applicable prevailing guidance, regulation, and law that mandates the nature in which pharmaceutical organizations function including but not limited to local health authority. 1-3. Lead Medical Communication/Publication and Exchange ■ Provide medical leadership and expertise to sales, marketing, legal and regulatory functions for marketed products and drugs in development. ■ Lead Publication strategy planning and its execution. Lead activities related to article publications, presentations at congresses and symposia ■ Provide medical review or support to the medical designee for scientific review and approval of promotional material and medical materials in compliance with corporate standards and government/ industry regulations. ■ Establish and maintain contact with Key Opinions Leaders (KOLs)/ Key Thought Leaders (physicians and researchers) with high level scientific and business communication skills within pertinent medical community ■ Lead to shape field strategies in line with global medical director group and local MSLs ■ Develop and maintain scientific relationships with KOLs/TLs to create awareness and understanding of the therapeutic area and products, and facilitate scientific exchange with KOLs ■ Fosters the establishment and maintenance of external scientific advisory boards and assists in advocacy development ■ Develop and leverage medical/scientific insights through attendance at scientific meetings to further develop own knowledge base in line with company and medical strategy, and remain informed of current developments within pertinent medical and scientific communities through familiarity with current literature, attendance at meetings, conventions, professional associations, ■ Conduct/attend/present at Advisory Boards initiated by the affiliate organization if there is a clear need for specific medical input ■ Support medical information role in alignment with medical information lead |
| 週勤務日数 | 5.0日 |
| 勤務時間 | (月～金) 09時00分 ～ 17時15分 フレックスタイム制あり |
| 当直 | なし |
待遇・手当
| 給与（年俸） | 1000万円 応相談 |
|---|---|
| 赴任手当 | - |
| 住宅手当 | - |
| 宿舎の提供 | - |
| 自動車通勤 | - |
福利厚生
| 休日 | 日曜日、祝日、土曜日 |
|---|---|
| 休暇 | 年末年始、その他休暇、初年度有給休暇 |
| 研究日 | なし |
| 社会保険 | 健康保険、雇用保険、労災保険、厚生年金 |
| 学会出席 | - |
その他
| 試用期間 | あり（3カ月）同条件 |
|---|---|
| 備考 | ・年収1000万円～（目安）※経験・スキルによります。 ・時間外労働あり ・社会保険：健康保険、厚生年金保険 ・労働保険：雇用保険、労働者災害補償保険 |
