临床数据经理

利用技术来影响患者并最终挽救生命，您是否有专业知识和对信息技术的热情？您是否想应用您的专业知识来影响遵循科学并将想法变成改变生活的公司的公司中的IT策略？如果是这样，阿欧洲杯微信买球斯利康可能是您的选择！关于阿斯利康欧洲杯微信买球阿斯利康（Astrazeeneca）是一家全球，以科学为主导的，以患者为中心的生物制药公司，重点介绍针对世界上一些最严重疾病的处方药的发现，开发和商业化。但是，我们不仅仅是世界领先的制药公司之一。在阿斯欧洲杯微信买球利康，我们致力于成为一个好地方。关于我们的IT团队，这是一个充满活力且以结果为导向的环境，但这就是我们喜欢它的原因。无论是在探索黑客马拉松的新技术，还是永远重新定义同事的角色和工作，都有无数的学习和成长机会。一路支撑塑造自己的路径。各种思想在功能和广泛地共同工作。 ABOUT THE ROLE - Study level CDM administrative support based on the relevant model and DM Vendor. This may include - but is not limited to activities related to the study start up, conduct and closeout phases. (i.e. - documentation review and/or creation, User Access Testing, query management, data cleaning and - reviews, third party data reconciliation in accordance with the project study model, KPIs and timelines.) - Day to day responsibilities may include but are not limited to - Study status reporting to the relevant clinical study team members, (e.g. provide data to clinical - teams for performing medical and clinical reviews, coordination of instream data review, lab - data review, etc.) - Collaboration with Data Management Vendor regarding upcoming deliverables and milestone - achievements (i.e., snapshots, interim, and migrations). - Oversight of the data quality, documentation quality, and types of these deliverables and milestones. - Responsible for the reporting in CDM specified systems and types of deliverables, achievement - achievements, risks and mitigations and data transfer agreements, and other study administrative - needs. - Responsible for the tracking of findings and outcomes (e.g. RCA and CAPA) to meet Quality Compliance - requirements. - Oversight of Trial Master File compliance for audit readiness. May include activities related to study - Expected Data Lists and quality compliance checks. - Performs User Acceptance Testing of internal and external electronic Data Capture systems as required. - Provides support to the resolution of issues related to Clinical Data Management deliverables and - inputting ideas to help resolve issues and contribute to continuous improvement Performs any CDM related ad-hoc requests from Line Manager or superior ESSENTIAL SKILLS REQUIRED University or college degree in the life sciences or related subject, pharmacy, nursing or equivalent relevant degree - Languages: Fluent English (oral and written) - Attention to detail to ensure quality - Good verbal and written skills - Ability to work flexibly on simultaneous projects and proactively manage time to meet own deadlines. - Strong interpersonal skills and proven ability to communicate effectively in a global environment. SO, WHAT’S NEXT? Are you already envisioning yourself joining our team? Good, because we’d love to hear from you! Click the link to apply and we’ll be in touch as soon as we can. WHERE CAN I FIND OUT MORE? Our Social Media, Follow AstraZeneca on LinkedIn https://www.linkedin.com/company/1603/ (https://www.linkedin.com/company/1603/) We are an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, sex, gender, gender expression, sexual orientation, age, marital status, veteran status, or disability status.

欧洲杯微信买球阿斯利康拥有多样性和机会平等。我们致力于建立一个包容性和多样化的团队，代表所有背景，并具有尽可能广泛的观点，并利用行业领先的技能。我们认为，我们的工作越多，我们的工作就会越好。我们欢迎并考虑申请加入所有合格候选人的团队，无论其特征如何。我们遵守有关就业（和招聘）不歧视的所有适用法律和法规，以及工作授权和就业资格验证要求。