- 常勤
- 東京都
【東京都・大阪府 大手外資系での就業】
【東京都／大阪府大阪市】大手外資系 神経内科・膠原病内科 週5日／1000万円～（目安の金額になります） ※経験・スキルによります。
- 300407474
- 2024年02月02日更新
- 当直なし
| 勤務地 | 東京都*** |
|---|---|
| 給与（年収） | 1000万円 応相談 |
| 募集科目 | 脳神経内科、リウマチ内科、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 | 脳神経内科、リウマチ内科、製薬会社 |
|---|---|
| 勤務内容 | その他 Scientific Advisor or Medical Advisor, Neurology Major Responsibilities: ・ Develop and maintain in depth knowledge for assigned product(s) / relevant therapeutic area(s) through attendance / participation at key internal meetings/training sessions, relevant congresses, and seminars and by regular self-study of the national/international literature. ・ Provide expert medical/scientific advice for assigned products and related therapeutic areas, including responding to requests for scientific/technical information; contribute to the development and medical and scientific accuracy of core dossiers generated by the medical department. ・ Establish and maintain professional and credible relationships with external experts and academic centers; this will involve participating in scientific congresses, coordinating advisory boards, round-table meetings, discussion forums, etc. ・ Deliver scientific presentations and medical education programs to healthcare professionals individually or in groups (meetings, clinical sessions, etc.), where requested. Develop and update medical education materials. ・ Screen relevant literature and other information from relevant scientific societies meetings and conferences and develop summaries of key messages for use within the Company (e.g. key areas of scientific/company interest, new trends in diagnosis, monitoring and treatments in the therapeutic area, etc.) ・ Contribute scientifically to train sales forces and other departments; develop and update relevant training materials. ・ Medical Research Activities: -Design and implement Medical research projects within defined standards and budgets (e.g. Phase IV, post marketing clinical activities such as registry/database projects, epidemiological surveys, and PMOS studies). -Provide the required oversight to manage review, approval and conduct of IIS studies. -Support the affiliate Clinical Research Department in the management of clinical studies, as appropriate (e.g. review new clinical study protocols, identifying potential investigators/sites, conducting feasibility surveys). ・ Review and preparation of promotional material. Ensure the medical/scientific content is correct and fully compliant with AbbVie’s internal policies and guidelines. ・ Provide medical/scientific input into marketing strategy and key commercial initiatives, as required. Monitor the environment for competitive intelligence (e.g. product strategies, studies, commercial messages, positioning, etc.) and communicate, where appropriate, within the Company. ・ Ensure compliance with all applicable national laws and regulations, guidelines, codes of conduct, AbbVie’s policies and procedures and accepted standards of best practice. |
| 週勤務日数 | 5.0日 |
| 勤務時間 | (月～金) 08時45分 ～ 17時30分 フレックスタイム制 ※コアタイム無 フレキシブルタイム5：00～22：00 休憩時間60分 |
| 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(10日) |
| 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カ月間）同条件 |
|---|---|
| 備考 | 【勤務地】東京都、大阪市 【給与】 年収1000万円～（目安の金額になります） ※経験・スキルによります。 |
