上海招聘

Responsibilities:

· Assist the clinical team to implement electronic document system and clinical trial management system in China. Assist with periodic review of system for accuracy and completeness

· Assist the clinical team in the preparation, handling, distribution, filing, and archiving of clinical documentation and reports according to the scope of work and standard operating procedures. Assist with periodic review of study files for accuracy and completeness.

· Assist Trial Supply Co-ordinator with preparation, handling and distribution of Clinical Trial Supplies and maintenance of tracking information.

Provide general office administration duties and related tasks.

Job Requirements:

· Degree in Science, with a major in Pharmacy, Biological / Life Sciences or Nursing from a recognized tertiary institution

· Minimum 1 year of clinical monitoring experience in the pharmaceutical / CRO industry.

· Strong written and verbal communication skills including good command of English language

· Strong software and computer skills, including MS Office applications

· Awareness of knowledge of applicable clinical research regulatory requirements; i.e.,Good Clinical Practice (GCP) and International Conference on Harmonisation (ICH) guidelines.

Good team work spirit and coordination skill

瑞石生物医药有限公司于2018年1月创立，总部位于中国上海，在北京及美国波士顿设有分支机构，是一家创新的研发驱动型全球生物制药公司，立足于开发临床急需的创新药物以满足患者的需求。目前，瑞石专注于自身免疫类疾病创新药物的全球开发，一方面与国内领先的制药企业恒瑞合作将中国创新药物引入美国及欧洲，助力中国创新走向世界；另一方面还借助公司管理团队在中国开展创新药物研发的丰富经验，积极引进国际领先的创新药物解决中国患者的临床需求。