CRM-Clinical Project Manager
Pharma-北京诺华制药有限公司
- 公司规模:500-1000人
- 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:2013-05-14
- 工作地点:北京
- 招聘人数:1
- 职位类别:临床研究员
职位描述
1. Plan and track of specific clinical activities within Development Greater China, from project initiation, protocol drafting to final study report writing.
2. Ensure that all project plan and timelines are in concert with regulatory colleagues and timelines to ensure maximum efficiency in new drug development for those clinical activities which are required for registration.
3. Lead China Project Team (CPT) to manage the cross function team to meet the specific development timeline.
4. Organize the regular China project team meeting, lead the team strategy discussion and take meeting minutes.
5. Be a counter-partner of GPTD. Keep daily connection with GPTD to understand latest strategy change and keep mutual communication transparent.
6. Coordinate with GPTD to organize the regular meetings between CPT and GPT.
7. Work with NIBR (CNIBR) to be familiar with the company's new product's pipeline, understand the products' development process and identify and develop appropriate products.
8. Manage the cross function team including Drug Regulatory Affairs (DRA), China Early Portfolio Strategy (CEPS) team members and Clinical Experts (CAs) to identify and develop promising portfolio compounds.
9. In association with Novartis global teams, ensure the highest quality in strategy inputs in DDP & FDP.
10. Undertake specific additional projects related to clinical development as may be required by the Clinical Franchise Head from time to time.
Required Knowledge and Skill (Physical and moral base)
- Significant training/experience [at least 5 years] in clinical development in the pharmaceutical industry including development project management/portfolio management and cross-functional working experience.
- Familiar with the process of drug development and life cycle management of a product in pharmaceutical industry
- Experience and knowledge in CVM therapy area would be a significant plus.
- Superior English writing, reading, speaking and listening skills and attention to detail
- Strong communication skills within a multidisciplinary team and in interfaces with other departments and headquarters
- Strong Sense of responsibility and dedication
- Teamwork spirit
- Skilful at Word/Excel/Access/PowerPoint/microsoft project.
2. Ensure that all project plan and timelines are in concert with regulatory colleagues and timelines to ensure maximum efficiency in new drug development for those clinical activities which are required for registration.
3. Lead China Project Team (CPT) to manage the cross function team to meet the specific development timeline.
4. Organize the regular China project team meeting, lead the team strategy discussion and take meeting minutes.
5. Be a counter-partner of GPTD. Keep daily connection with GPTD to understand latest strategy change and keep mutual communication transparent.
6. Coordinate with GPTD to organize the regular meetings between CPT and GPT.
7. Work with NIBR (CNIBR) to be familiar with the company's new product's pipeline, understand the products' development process and identify and develop appropriate products.
8. Manage the cross function team including Drug Regulatory Affairs (DRA), China Early Portfolio Strategy (CEPS) team members and Clinical Experts (CAs) to identify and develop promising portfolio compounds.
9. In association with Novartis global teams, ensure the highest quality in strategy inputs in DDP & FDP.
10. Undertake specific additional projects related to clinical development as may be required by the Clinical Franchise Head from time to time.
Required Knowledge and Skill (Physical and moral base)
- Significant training/experience [at least 5 years] in clinical development in the pharmaceutical industry including development project management/portfolio management and cross-functional working experience.
- Familiar with the process of drug development and life cycle management of a product in pharmaceutical industry
- Experience and knowledge in CVM therapy area would be a significant plus.
- Superior English writing, reading, speaking and listening skills and attention to detail
- Strong communication skills within a multidisciplinary team and in interfaces with other departments and headquarters
- Strong Sense of responsibility and dedication
- Teamwork spirit
- Skilful at Word/Excel/Access/PowerPoint/microsoft project.
公司介绍
北京诺华制药有限公司开发、生产和销售治疗多种疾病的创新处方药,涵盖的疾病领域包括:心血管、内分泌、肿瘤、抗感染、风湿疼痛及骨质疏松、移植免疫、中枢神经以及眼科。北京诺华制药曾获得“***雇主”和“最负社会责任的企业”等殊荣。
“诺华”中文取意“承诺中华”,即承诺通过不断创新的产品和服务致力于提高中国人民的健康水平和生活质量。北京诺华制药成立于1987年,总部设在北京,隶属于瑞士诺华公司。
诺华公司致力于为患者及社会提供创新医药保健解决方案,以满足其日益变化的健康需求。2011年,集团持续经营业务实现净销售586亿美元。集团研发投入约为96亿美元(去除减值及摊销后为92亿美元)。诺华集团总部位于瑞士巴塞尔,业务遍及全球140多个国家和地区,拥有124,000位全职员工。诺华集团立足在中国的长期发展,重要战略投资包括位于上海的综合性生物医学研发中心,以及位于北京昌平的制剂生产工厂和江苏常熟的原料药生产工厂。如需更多信息,敬请登录公司网站http://www.novartis.com和http://www.novartis.com.cn。
“诺华”中文取意“承诺中华”,即承诺通过不断创新的产品和服务致力于提高中国人民的健康水平和生活质量。北京诺华制药成立于1987年,总部设在北京,隶属于瑞士诺华公司。
诺华公司致力于为患者及社会提供创新医药保健解决方案,以满足其日益变化的健康需求。2011年,集团持续经营业务实现净销售586亿美元。集团研发投入约为96亿美元(去除减值及摊销后为92亿美元)。诺华集团总部位于瑞士巴塞尔,业务遍及全球140多个国家和地区,拥有124,000位全职员工。诺华集团立足在中国的长期发展,重要战略投资包括位于上海的综合性生物医学研发中心,以及位于北京昌平的制剂生产工厂和江苏常熟的原料药生产工厂。如需更多信息,敬请登录公司网站http://www.novartis.com和http://www.novartis.com.cn。
联系方式
- Email:staffing.center@novartis.com
- 公司地址:上班地址:建国门外大街1号国贸大厦2座