临床数据监察员
职位描述
PRINCIPAL DUTIES AND RESPONSIBILITIES: Indicate key areas of responsibility, major job duties, special projects and key objectives for this position. These items should be evaluated throughout the year and included in the written annual evaluation.
The Clinical Data Supervisor will:
1. Analyze the enrollment status and alert the clinical program manager if unusual activities or absences of activities are detected
2. Verify accuracy of case report forms against study protocol
3. Monitor clinical data entry time and completeness based on scheduled clinical visits during a trial
4. Review laboratory data periodically and identify any laboratory values that are significantly outside the normal range.
5. Perform initial assessment to determine whether the abnormal values may result from a laboratory error or may be clinically significant and alert appropriate clinical project team members accordingly.
6. Review inclusion and exclusion criteria, medical history, demographics and or other baseline characteristics of study subjects to alert team to any eligibility violation
7. Review adverse event data and concomitant medication use to detect unusual or absent activities. Identify outliers in safety data pattern.
8. Review and revise adverse event and medication coding for consistency and accuracy
9. Perform periodic pharmacovigilance analysis to detect safety signals
10. Generate graphs and reports using spreadsheet and database tools
QUALIFICATIONS:
1. Bachelor of Medicine or related Life Science discipline, or higher
2. Completed courses in biochemistry and human physiology
SKILLS/ ABILITIES/ COMPETENCIES REQUIRED: (MUST be realistic, measurable, objective, and related to the essential functions of the job.)
1. Proficient in English reading and verbal communication
2. Proficient in Microsoft Excel and data table manipulations
3. Familiar with statistical methods for data analysis
4. Familiar with medical terms and laboratory testing principles
5. Familiar with database structure and electronic data capture is a plus
企业简介
白鹭医药技术(上海)有限公司[Egret Pharma (Shanghai) Ltd.] 位于著名的上海“张江药谷”,于2003年注册,是一家由美中医药界知名企业家、科学家团队创办的美资企业。公司致力于创新药物的研究和开发,立志在中国打造出具有自主研发能力的国际化现代药物企业。
公司创始人及管理团队来自国际医药界知名的企业家和学术科研精英。他们熟悉行业的国际市场运行环境及运行规则,并有成功创办NASDAQ上市公司的经验。管理团队成员(CEO,CSO,COO)在美国跨国制药公司有10年以上药物研发和管理经历,在新药开发领域,如现代药物化学、组合化学、药物设计、ADME、动物试验、临床试验及研发管理等方面有独特的技术优势。为确保公司的研发工作处于世界一流水平,公司还聘请欧美主流医药界之资深专家担任公司的长期顾问。公司建立有符合国际一流标准的软硬件系统及管理体系,拥有先进的现代药物研究设备和实验条件,以及一流的文献检索数据库和信息管理系统,并已全面实现科研工作信息的电子化管理。
目前,药物的知识产权问题引起了中国政府乃至社会各界的广泛关注,新药创制领域有着广阔的发展空间;公司以上海为立足点,将市场目标定位于整个中国市场及欧美主流市场;加之公司的人才、技术优势,以及开放、高效、和谐的人文环境;白鹭医药可谓“天时、地利、人和”。
热门区域招聘: 重庆 北京 上海 浙江 江苏 广东 山东 湖南 安徽 河北
上海招聘企业: 百进冠合(海南) 医疗科技有限公司 上海华茂药业有限公司 上海信谊药厂有限公司 上海强生制药 欧姆龙健康医疗(中国)有限公司 青海瑞成药业(集团)有限公司 上海交通大学医学院附属瑞金医院 复旦大学附属中山医院 上海复星医药 上海医药集团
职位发布日期: 2016-03-24