Sourcing Supervisor-6 month contractor
北京诺华制药有限公司
- 公司性质：外资(欧美)
- 公司行业：制药/生物工程
职位信息
- 发布日期：2013-07-11
- 工作地点：上海
- 招聘人数：1
- 工作经验：三年以上
- 学历要求：本科
- 语言要求：英语熟练
- 职位类别：采购主管 生物工程/生物制药
职位描述
Job Purpose
Within the Greater China Region to provide Sourcing support for Development. In particular working with global category leaders to direct the utilization of Contract Research Organizations (CROs), Central Labs. and Specialty Providers to assure the delivery of quality, timely and cost-effective external resources to support the Novartis Development pipeline. Lead projects, working groups, initiatives to develop effective sourcing strategies for the Greater China Region and ensure Clinical Contracting Excellence (CCE) is delivered to successfully respond to the changing needs & requirements - legal, operational, regulatory & financial - of our internal & external customers, worldwide. Provides Sourcing and Logistical support to all Development Line Functions within China
Major Activities
1. Establishes and maintains a Professional Sourcing Function.
2. Lead the selection of the optimum External Service Provider (ESP) {CRO, Central/ Reference Lab, and Specialty provider} at both the tactical and strategic level based on fit for purpose, or value added services, cost avoidance and savings opportunities and in particular, to build detailed understanding and represent Chinese vendors and supply market capabilities in evolving global sourcing strategies.
3. Train Clinical Teams in outsourcing procedures, assist Clinical Teams in defining the scope of work, and in some cases define the scope of work for both original contract and contract amendments.
4. Negotiate contract terms, scope of work, pricing and payment schedules, ensuring that the agreements with the ESPs are commercially advantageous to Novartis, while minimizing regulatory, legal, and financial risks through close collaboration with functional partner such as legal, Finance, QA, and functional lines
5. Produce final contracts/amendments and secure all necessary company approvals including compliance with local and global SOP's, to facilitate execution of said agreements
6. Manage ongoing vendor performance and contract delivery (business conflicts, issue resolution, performance management)
7. Manage the interface between China Development and Development Category Management and Global Contract Management, internal key stakeholders and where appropriate ESPs to enhance the success of outsourced trials and to ensure implementation of best practice in China.
8. Support the MSA(s) language and commercial terms e.g. rates negotiations for Strategic and non-Preferred ESPs using best practice tools like category management, total cost of ownership and e-procurement tools.
9. Contribute to vendor audit requests and follow-up corrective action plans as required
10. Ensure ESPs are delivering in line with expectations.
11. Lead and develop effective relationships within Development China and Development Strategic Sourcing and actively participate in network opportunities and meetings to deliver Development objectives.
12. Responsible for Import / Export of samples, equipment etc.
Ideal Background
Education (minimum/desirable): Bachelor's Degree in Science / PhD, Business Degree or equivalent
commercial experience desirable.
Languages: Fluent English - Oral and written
Chinese (Mandarin) - Oral and written
Experience/Professional requirement:
1. At least 3-5years experience in Drug Development in Pharmaceutical Industry or with a Central Laboratory in addition 1-2 years of Sourcing or similar commercial experience
2. Good understanding of the clinical development process and very robust understanding of the management of clinical trials
3. Project management skills
4. Good influencing and negotiation skills.
5. Solid understanding of contracts (including solid legal understanding of terms and conditions).
6. Familiar with the CRO/Central Laboratories/ReferenceLaboratories and Specialty Provider marketplace.
7. Financial understanding (understanding of cost drivers for clinical trials) as it relates to contracts and cost reductions.
8. Excellent written and oral communications skills (English and Chinese / Mandarin).
9. Strong problem solving skills.
10. Strategic thinker
11. Demonstrated willingness to make decisions and to take responsibility for such.
12. Ability to address issues assertively while maintaining a non-threatening posture
13. Excellent interpersonal skills (team player).
Within the Greater China Region to provide Sourcing support for Development. In particular working with global category leaders to direct the utilization of Contract Research Organizations (CROs), Central Labs. and Specialty Providers to assure the delivery of quality, timely and cost-effective external resources to support the Novartis Development pipeline. Lead projects, working groups, initiatives to develop effective sourcing strategies for the Greater China Region and ensure Clinical Contracting Excellence (CCE) is delivered to successfully respond to the changing needs & requirements - legal, operational, regulatory & financial - of our internal & external customers, worldwide. Provides Sourcing and Logistical support to all Development Line Functions within China
Major Activities
1. Establishes and maintains a Professional Sourcing Function.
2. Lead the selection of the optimum External Service Provider (ESP) {CRO, Central/ Reference Lab, and Specialty provider} at both the tactical and strategic level based on fit for purpose, or value added services, cost avoidance and savings opportunities and in particular, to build detailed understanding and represent Chinese vendors and supply market capabilities in evolving global sourcing strategies.
3. Train Clinical Teams in outsourcing procedures, assist Clinical Teams in defining the scope of work, and in some cases define the scope of work for both original contract and contract amendments.
4. Negotiate contract terms, scope of work, pricing and payment schedules, ensuring that the agreements with the ESPs are commercially advantageous to Novartis, while minimizing regulatory, legal, and financial risks through close collaboration with functional partner such as legal, Finance, QA, and functional lines
5. Produce final contracts/amendments and secure all necessary company approvals including compliance with local and global SOP's, to facilitate execution of said agreements
6. Manage ongoing vendor performance and contract delivery (business conflicts, issue resolution, performance management)
7. Manage the interface between China Development and Development Category Management and Global Contract Management, internal key stakeholders and where appropriate ESPs to enhance the success of outsourced trials and to ensure implementation of best practice in China.
8. Support the MSA(s) language and commercial terms e.g. rates negotiations for Strategic and non-Preferred ESPs using best practice tools like category management, total cost of ownership and e-procurement tools.
9. Contribute to vendor audit requests and follow-up corrective action plans as required
10. Ensure ESPs are delivering in line with expectations.
11. Lead and develop effective relationships within Development China and Development Strategic Sourcing and actively participate in network opportunities and meetings to deliver Development objectives.
12. Responsible for Import / Export of samples, equipment etc.
Ideal Background
Education (minimum/desirable): Bachelor's Degree in Science / PhD, Business Degree or equivalent
commercial experience desirable.
Languages: Fluent English - Oral and written
Chinese (Mandarin) - Oral and written
Experience/Professional requirement:
1. At least 3-5years experience in Drug Development in Pharmaceutical Industry or with a Central Laboratory in addition 1-2 years of Sourcing or similar commercial experience
2. Good understanding of the clinical development process and very robust understanding of the management of clinical trials
3. Project management skills
4. Good influencing and negotiation skills.
5. Solid understanding of contracts (including solid legal understanding of terms and conditions).
6. Familiar with the CRO/Central Laboratories/ReferenceLaboratories and Specialty Provider marketplace.
7. Financial understanding (understanding of cost drivers for clinical trials) as it relates to contracts and cost reductions.
8. Excellent written and oral communications skills (English and Chinese / Mandarin).
9. Strong problem solving skills.
10. Strategic thinker
11. Demonstrated willingness to make decisions and to take responsibility for such.
12. Ability to address issues assertively while maintaining a non-threatening posture
13. Excellent interpersonal skills (team player).
公司介绍
诺华正在通过创想医药未来，改善人们的生活质量、延长人类的寿命。作为全球知名的医药健康企业，我们运用创新科学和数字化技术，在医药健康需求增长的领域创造变革性的治疗方法。在探索新药物的过程中，我们不懈创新，对研发的投资一直处于行业全球先列。在全球，近8亿患者受益于诺华产品，同时，我们持续探索更多创新方式使我们的创新疗法造福更多患者。诺华在全球拥有来自超过140个国家的约11万名员工。
诺华在中国的经营活动可追溯到200多年前。早在1886年，嘉基公司就开始在中国推广染料，此后汽巴公司与山德士公司也先后进入中国市场。1970年，嘉基公司和汽巴公司合并；并于1987 年在华成立北京汽巴-嘉基制药有限公司，这就是北京诺华制药有限公司的前身。1996年，汽巴-嘉基和山德士合并成为诺华公司诺华在中国的业务包括诺华肿瘤、诺华制药和山德士，全国建有两大生产基地，并在北京、上海和江苏设立了研发机构。从研发到生产销售，诺华以多元化的业务组合，全面服务中国老百姓的健康。目前，诺华在中国拥有8000多名员工。
关注诺华招聘公众号，创想职业精彩未来！
诺华在中国的经营活动可追溯到200多年前。早在1886年，嘉基公司就开始在中国推广染料，此后汽巴公司与山德士公司也先后进入中国市场。1970年，嘉基公司和汽巴公司合并；并于1987 年在华成立北京汽巴-嘉基制药有限公司，这就是北京诺华制药有限公司的前身。1996年，汽巴-嘉基和山德士合并成为诺华公司诺华在中国的业务包括诺华肿瘤、诺华制药和山德士，全国建有两大生产基地，并在北京、上海和江苏设立了研发机构。从研发到生产销售，诺华以多元化的业务组合，全面服务中国老百姓的健康。目前，诺华在中国拥有8000多名员工。
关注诺华招聘公众号，创想职业精彩未来！