Head of Medical Affairs Oncology

Posted 19 Oct 2022

Taipei, T'ai-pei - Taiwan

Req Id 257251

 

在默克我們企業,的職業生涯是一段不斷探索的旅程:我們約 60,300 名員工正透過新一代的先進醫療保健、生命科學與電子科技,塑造全球的生活、工作和娛樂方式。350 多年的歷史與遍及全球的軌跡,我們熱切地推動我們的好奇心,以便找到創新和充滿活力的方式來改善他人的生活。

 

在醫藥健康領域,我們團結一致,齊心為病患,幫助孕育、改善和延長生命。這是我們的目標,也是我們每天不懈努力的原因。默克在腫瘤、神經變性疾病和輔助生殖等領域不斷開發創新藥物、智慧設備與創新科技。我們的團隊遍佈全球六大洲,在共同的理念與好奇心驅動下,我們全力以赴地為處於生命各個階段的患者提供擁抱新生活的機會。加入我們,成為這個多元、包容、靈活工作文化的一份子,並獲得在全球範圍內的個人職業發展機會。

 


 

Roles responsible for ensuring compliance with pharmaceutical regulations and laws as well as providing expertise on drug safety. Provides medical expert advice to ensure accuracy of data to support existing or new product promotion. Develops medical product information and stays informed on scientific trends and competition. Maintains relationships with target opinion leaders and trains local teams in medical topics.

 

Your Role:

 

1. Medical Management and Leadership:

- Responsible for assigning, tracking and monitoring relevant KPIs and metrics for Medical affairs Department.

- Launch and Brand Strategies and lead the Medical Affairs Tactics Talent Management and People Development

    - Manage a broad portfolio of Medical Affairs tactics, across therapeutic areas for assets at various stages of the lifecycle (ie phase 4 studies, med ed, field medical etc)

    - Consolidate and share healthcare landscape (payor, patient, access) insights and translate those insights into affiliate strategies,

    - Lead affiliate yearly budget and business planning, prioritization and trade-offs

 

2. Regulatory & Compliance Management:

- Successfully collaborate and lead resolution of regulatory, reputational, compliance and other risk issues in the affiliate

- Deliver on post-marketing commitments on time and with quality

- Manage ethical issues at affiliate to resolutions that satisfy business and societal needs

- Participate in and contribute significantly to internal policy and external trade or regulatory working teams on matters that impact the affiliate

 

3. Scientific and Technical Leadership:

- Actively inform and contribute to GMA/RMA and local strategy and tactics in collaboration with Global/Regional TA’s, GME and General manager

- Collaborate with pharmacovigilance and regulatory in interpreting regulatory and safety risks in their geography

- Provide counsel on clinical and health outcomes research design and ensure that the Country research proposals are scientifically and strategically aligned to global data generation priorities (Country Council)

- Organize and Chair the Country R&D Council and Local Quality and Safety Team (LQST)

 

Who you are:

 -5-7 years in pharmaceutical industry (at least significantly in Medical Affairs roles)      

 -University degree (Bachelor’s) required, preferably in scientific field of relevance to position

 -Secondary / advanced scientific degree (e.g., PharmD, PhD, DO, MD, MBBS) required

     -Proven training/experience in Clinical or Basic Research, Epidemiology,Pharmacoeconomics, Clinical Pharmacology and/or Administration is advantageous

     -Good understanding of local compliance and regulatory requirements for pharmaceutical Medical Affairs, R&D and Commercial work

     -Experience in other pharmaceutical functions in local, regional or global/ Regional roles desirable

     -Experiences in clinical practice as licensed specialist preferred

     -Local recognition or credibility among External Experts (KOLs) preferred

 


 

我們提供:我們充滿好奇心的團隊是由多元的背景、觀點和生活經驗所組成。我們宣揚多元的各個面向。我們相信,就是這樣的多元推動了卓越、創新和人類進步。我們關心我們的客戶、患者和各式各樣的人們。這種多元強化了我們在科技領域中的領導能力。 我們致力於為所有人創造機會,並賦能實現妳的誌向。我們的各大事業單位提供了各種職涯發展機會並拓展妳的視野。 加入我們壹起打造可影響數百萬人的包容性和歸屬感文化,讓每個人都能將自己的好奇心實現成真!


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