Clinical Data Analyst
职位描述
职位描述:
The role of the Clinical Data Analyst (CDA) is to perform all clinical data cleaning activities on
assigned projects, commensurate with experience and/or project role. Key activities include data
validation, generation and integration of queries, coding of clinical data, reconciliation of safety and
electronic data.
The Clinical Data Analyst will assume the Clinical Data Manager responsibilities on studies that started
Key Accountabilities
??Utilize current study documentation including protocol, Case Report Forms (CRFs), Cleaning
guidelines etc.
??Conduct in-house data review
??Generate and close queries or apply self evident corrections to the data according to the relevant
guidelines
??Identify and report protocol violations
??Manual and Patient Profile review, issue queries
??Conduct reconciliation of SAEs, send out queries as required and notify relevant Safety Groups
of possible issues for their action
??Track and integrate queries
??Perform clinical coding if appropriate to role within the project team
??Ensure all documents coded for submission to central files
??Lock site(s) within EDC system - remove user's data modification privileges
??Interact with site (via mail) as required
??Perform early and final database QC activities
??Update all relevant tracking system on an ongoing basis
??Inform responsible CDA coordinator of work status regularly
??Keep manager informed about work progress and any issues to avoid surprises. Requires
regular interaction / supervision by Manager or assigned mentor
??Maintain a working knowledge and ensure compliance with applicable ICH-GCP Guidelines,
local regulatory requirements and PAREXEL WSOP and stud specific procedure
??Complete routine administrative tasks in a timely manner (e.g. timesheets, metrics, travel
expense claims
Skills
??Good computer skills including but not limited to the knowledge of Clinical Trial/Data
Management Systems, PMED, MS-Office products such as Excel, Word.
??Demonstrate a sound awareness of all relevant regulations, including GCP
??Ability to successfully work in a (‘virtual’) team environment
??Client focused approach to work
??If required, knowledge of medical terminology and awareness of coding dictionaries (e.g.
MedDRA & WHODRUG)
??Solid interpersonal, verbal and written communication skills
??Sense of urgency in completing assigned tasks
??Meticulous attention to detail
??Effective time management in order to meet daily metrics or team objectives
??Shows commitment to and performs consistently high quality work
Education
??Bachelor’s degree and / or other medical qualification or relevant DM experience
Language Skills
??Competent in written and oral English
企业简介
公司简介:
国际精鼎科技股份有限公司(APEX International Clinical Research Co., Ltd. ), 成立于1996年,系协助世界各国大药厂从事新药开发及临床试验的临床研究委托机构(Contract Research Organization)。
国际精鼎临床试验研究团队是由一群具有丰富跨国性临床试验经验及专业知识的精英所组成,目前已成为亚洲地区规模最大、服务项目最完整之专业CRO公司,幷已在业界建立高品质的专业形象以及良好口碑。
APEX目前拥有超过300名的专业精英,服务遍及11个国家,在CRO的领域里已是亚洲的领导先驱。预计2007年APEX服务版图将再扩及2个国家、4个服务据点,人员也将扩增至500人。APEX重视与客户的承诺,更重视人才的培育和养成,我们提供完整的教育训练、职涯规划、优于市场的薪资福利、良好工作环境,期许同仁与公司一同成长,迈向未来。
主要服务项目:
新药开发策略的拟定与计划
国际临床试验规划及整合
引荐、甄选试验计划主持人
受试者同意书之设计
人体试验委员会之送审
最高卫生主管机关之送审
临床试验护理专员
临床研究数据处理
向亚洲地区卫生主管机关办理新药查验登记事务
中草药及健康食品临床试验、法规咨询及查验登记
愿景(Vision):创造一个在亚太地区具有国际竞争力的最精良CRO团队。
发展使命(Mission):
1 争取国际大药厂委托,执行符合国际水准的跨国性临床试验。
2 协助亚太生技及制药产业建立新药开发模式,以提升产品研发能力,幷促使产品国际化。
3 以提升临床试验品质为宗旨,拓展全球市场为目标,整合计算机及通讯科技,在国际上提供客户兼具成本效益及效率的临床试验数据处理中心。
4 建立一个以亚洲人种高发生率疾病的基因数据库,以提供国际性新药研发机构所须之基因信息,协助其缩短药物开发时程,幷提高研发成功率。
福利制度:
.薪资:
1. 提供具竞争性之薪资(含车补及饭补)
.保险类:
1. 社会保险(依照国家规定)及住房公积金
2. 团体保险(包括寿险、意外暨医疗保险)
.制度类:
1. 学习发展计划 (Learning & Development): 针对个别员工之专业及兴趣,设计符合其个人之生涯规划
2. 完整的教育训练:每年公司均针对所有员工,提供完整之教育训练
3. 顺畅的升迁管道及可转调其它部门;如有职缺,亦可申请调至海外各子公司
.请 / 休假制度:
1. 服务第一年即享有9天特休, 后续年休假天数则依据服务年资及公司制度而定
2. 一年可享4天不扣薪病假
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: 2016-12-09