At Johnson & Johnsonwe believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented treated and curedwhere treatments are smarter and less invasive andsolutions are our expertise in Innovative Medicine and MedTech we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow and profoundly impact health for more at
Job Function:
Medical Affairs Group
Job Sub Function:
Medical Affairs
Job Category:
People Leader
All Job Posting Locations:
Chuo-ku Tokyo Japan
Job Description:
Essential Job Functions
Building Clinical evidence
- Identify clinical trial needs based on clinical strategy
- In collaboration with each stakeholder such as the facility Study Secretariat and CRO test execution and management
- rofessional Education Program
- As part of our physician education program Negotiate with KOL and cooperate with internal and external stakeholders to execute and manage operations
- Planning and implementation of internal education programs
Provision and distribution of Clinical information
- Incollaboration with the Global team we plan and run an academic information sharing program for Japanese physicians academic conferences literature materials Support for content creation
Requirements
- At least 5 years of clinical development or medical affairs experience at a pharmaceutical company medical device manufacturer or CRO
- Project Manager or monitor experience in doctor-initiated trials clinical trials etc.
- Knowledge of basic diseases and treatments in the cardiovascular area
- English: Business-level literacy
- Great verbal and written communication skills
- Logical and strategic thinking
- Be willing to accumulate academic knowledge continuously
- Ability to work in a fast-paced environment while managing multiple priorities is preferred.
Essential Job Functions
Clinical Evidence 構築
- 臨床的戦略に基づき臨床試験ニーズの発掘
- 施設やStudy事務局CROなど各Stakeholderと連携し試験遂行と管理
Professional Education Program
- 医師向けの教育プログラムを遂行するにあたりKOLとの交渉及び社内外の関係者と協力し業務実行と管理
- 社内向けの教育プログラムの企画実行
- 情報の提供及び配信
- Globalチームと連携し日本の医師向けの学術的な観点からの情報共有プログラム企画運営
- 学会文献等資料コンテンツ等作成支援
Requirements
- 製薬会社医療機器メーカーCROのいずれかで臨床開発又はメディカルアフェアーズでの5年以上の経験者
- 医師主導試験治験臨床治験等でのProject Managerもしくはモニター経験がある
- 循環器領域での基本的な疾患及び治療の知識がある
- 英語ビジネスレベルで読み書きができる方
- コミュニケーション能力の高い方
- 論理的かつ戦略的な思考力
- 継続的な学術知識の集積意欲があること
Required Experience:
Manager
At Johnson & Johnsonwe believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented treated and curedwhere treatments are smarter and less invasive andsolutions are our expertise in Innovative Medicine and MedTech we are unique...
At Johnson & Johnsonwe believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented treated and curedwhere treatments are smarter and less invasive andsolutions are our expertise in Innovative Medicine and MedTech we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow and profoundly impact health for more at
Job Function:
Medical Affairs Group
Job Sub Function:
Medical Affairs
Job Category:
People Leader
All Job Posting Locations:
Chuo-ku Tokyo Japan
Job Description:
Essential Job Functions
Building Clinical evidence
- Identify clinical trial needs based on clinical strategy
- In collaboration with each stakeholder such as the facility Study Secretariat and CRO test execution and management
- rofessional Education Program
- As part of our physician education program Negotiate with KOL and cooperate with internal and external stakeholders to execute and manage operations
- Planning and implementation of internal education programs
Provision and distribution of Clinical information
- Incollaboration with the Global team we plan and run an academic information sharing program for Japanese physicians academic conferences literature materials Support for content creation
Requirements
- At least 5 years of clinical development or medical affairs experience at a pharmaceutical company medical device manufacturer or CRO
- Project Manager or monitor experience in doctor-initiated trials clinical trials etc.
- Knowledge of basic diseases and treatments in the cardiovascular area
- English: Business-level literacy
- Great verbal and written communication skills
- Logical and strategic thinking
- Be willing to accumulate academic knowledge continuously
- Ability to work in a fast-paced environment while managing multiple priorities is preferred.
Essential Job Functions
Clinical Evidence 構築
- 臨床的戦略に基づき臨床試験ニーズの発掘
- 施設やStudy事務局CROなど各Stakeholderと連携し試験遂行と管理
Professional Education Program
- 医師向けの教育プログラムを遂行するにあたりKOLとの交渉及び社内外の関係者と協力し業務実行と管理
- 社内向けの教育プログラムの企画実行
- 情報の提供及び配信
- Globalチームと連携し日本の医師向けの学術的な観点からの情報共有プログラム企画運営
- 学会文献等資料コンテンツ等作成支援
Requirements
- 製薬会社医療機器メーカーCROのいずれかで臨床開発又はメディカルアフェアーズでの5年以上の経験者
- 医師主導試験治験臨床治験等でのProject Managerもしくはモニター経験がある
- 循環器領域での基本的な疾患及び治療の知識がある
- 英語ビジネスレベルで読み書きができる方
- コミュニケーション能力の高い方
- 論理的かつ戦略的な思考力
- 継続的な学術知識の集積意欲があること
Required Experience:
Manager
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