长沙招聘

Major Accountabilities (Describe the main results of the job to be achieved )
1.Hire, train, supervise team of CRAs and allocate trials in assigned territory.
2.Assure that required level of knowledge and skill is present and trials sites are monitored as per SOPs.Identify skills and competency gaps.Work with training team to develop training plans and coordinate training as needed.
3.Develop territory by identifying and screening new sites for participation in assigned clinical trials.
4.Monitor on status of planned versus actual patient recruitment and implement strategies to correct deviations from proposed plan according to metrics.Ensure that project time lines and quality targets are met for all trials to support product registration/marketing support.
5.Ensure that prevailing legislation, GCP and SOP requirements are fulfilled.
6.Work to coordinate for audits.
7.Liaise with global TA/BU clinical teams (e.g.escalates unresolved site issues) and CPO colleagues to enhance Novartis relationship with clinical sites.
8.Manage and direct the monitors with problem solving at the site level where needed.
9.Set and meet specific targets for responsible clinical trial budget and patient recruitment
10.Provides operational input to Clinical Trial Protocols, CRFs and Data Management meetings as required
11.Sets objectives and conducts individual monitor's performance reviews and makes salary recommendations
12.Leads, motivates and develops staff to improve and maintain their individual performance and that of their monitoring group as a whole
13.Provides training and coaching to CRAs with regard to all aspects of the drug development and clinical trial process
14.Coach and provide guidance to the staff to be compliant:

Ideal Background (State the minimum and desirable education and experience level)
Education:A degree in scientific or health discipline required
Languages:Fluent English (oral and written).
Experience:Expert in a specific disease area with established requirement: contacts in the medical community.
At least 6 years experience in clinical research with proven proficiency in trial execution and drug development.

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。