1. Reads and analyzes protocol, statistical analysis plan, CRF and other trial design documents and discusses with other team members such with as biostatisticians and data managers.
2. Develops and debugs simple to complex SAS program in a timely manner
3. Implements statistical analysis plan, data preparation, and data manipulation into SAS programs and macros
4. Create analysis datasets, statistical tables, figures, and listing for clinical trial data.
5. Create CDISC standard datasets (SDTM and ADaM)
6. Participates in the validation of SAS programs and analysis datasets
7. Maintains documentation for SAS programs and validation results
8. Leads and coordinates the programming work for projects involving SAS programming if necessary
9. Coordinates timelines in orders to fulfill the needs of other departments
1. Design CRF based on study protocol and prepare the CRF completion guideline.
2. Generate data management plan and data validation plan.
3. Clinical Data Management / Clinical data management status report.
4. Provide training to the site personnel and reporting agencies on proper data collection processes.
5. Coordinate with clinical monitoring activities to help provide prompt feedback to sites on data quality.
6. Establish data quality standards and works with reporting agencies to ensure standards are met.
7. Generate and close queries or apply self evident corrections to the data according to the relevant guidelines.
Primary Function of Position:
The Contingent Research Data Analyst, based out of Taiwan, will provide research, analytic, and data management support to the Ion Custom Hospital Analytics (Ion CHA) team. Ion CHA uses hospital-provided patient care data to assess the impact of the Ion lung biopsy platform on lung cancer treatment programs. The research analyst will work remotely with health services researchers and market access specialists to generate and answer research questions by independently analyzing healthcare data. The research analyst will also support data cleaning and visualization activities for Ion CHA.
Roles & Responsibilities:
• Data Management and Visualization
o Using a scripting language such as R, write code to clean data, create derived variables, merge/join/concatenate tables, identify missing values and outliers, and identify data inconsistencies.
o Visualize healthcare data by creating data dashboards with charts and tables by leveraging tools such as Tableau, R-Shiny, Quarto, ggplot2, and plotly.
o Automate data reports to share with internal and external stakeholders, including market access specialists and hospital executives.
• Research and Analysis
o Explore electronic health record data (EHR) and other large healthcare datasets to answer business questions related to cancer outcomes and costs.
o Use statistical and research design methodology to identify significant differences between patient cancer treatment pathways.
o Support the development of research publications and conference abstracts.
• Additional Project Support
o As needed support GAVE team with additional data analytic and visualization projects based on analyst interests and team needs.
*此為Adecco外包職缺,合約期間為半年,後續將依表現與營運視況延長*
*歡迎將履歷郵寄至Maggie.huang@adecco.com
【Job description】
This role also needs to manage data platform including customer, performance and digital channels to support data consolidation, alignment and analytics.
- Data and platform management and enhancement
- Understand deeply of company’s data bases with the capabilities to manage data base with accuracy and efficiency.
- Pilot, accelerate and maintain digital channels and platforms to support company data and digital strategy.
- Contact window of region or global for platform governance and enhancement.
- Data consolidation
- Organize, manage, and deliver data consolidation form different sources and platform to provide comprehensive review in support business analytic team.
- To generate data in supporting digital engagement performance tracking.
- Introduce contemporary data security, data privacy.
【Ideal Background】
1. 1 year experience in analytics or data science in the FMCG/Tech/Healthcare / Biotech/ OTC companies with strong knowledge of statistics, visualization, data preprocessing, and data analytics. Pharma Company is a plus.
2. Proficiency with data mining, mathematics, and statistical analysis
3. Experience with Excel, PowerPoint, SQL, and Power BI.
4. Strong communication and good team player, and able build alignments
5. Strong technical skills, data-driven and result-oriented thinking
6. Fluent in English and Mandarin
【 Job Description】
 Responsible for clinical trial data management, including database design, validation, and maintenance
 Draft and review Data Management Plan (DMP), Edit Check Specification, and other related documents
 Perform data cleaning, and collaborate with CRA/CRC and biostatistics teams to ensure data accuracy and integrity
 Handle data import, coding (e.g., medication, AE/SAE coding), and database lock procedures
 Support the use and maintenance of data management systems (e.g., Medidata Rave, Oracle Clinical)
 Collaborate with global teams, with strong English communication skills required; Japanese proficiency is a strong plus
【Requirement】
 Bachelor’s degree or above in life sciences, pharmacy, biostatistics, public health, or related fields
 Minimum 2 years of experience in clinical data management (CRO or pharmaceutical industry experience preferred)
 Familiar with ICH-GCP and clinical data management processes
 Fluent English communication skills (written and spoken) are required
 Japanese proficiency is a strong advantage
【 應徵方式 】
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- 方法二:直接投遞給我們https://reurl.cc/0W43pA
*****小提醒*****在介紹自己的部分,告訴我們想看 CDM 的職位
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Line: @ghchunting
AIBEDA is a Contract Research Organisation (CRO) specialising in medtech and AI-powered healthtech innovation. The company provides end-to-end services, including regulatory strategy, clinical protocol design, technology assessment, and market entry support, to help clients navigate the global regulatory landscape. With a focus on agility, data-driven insights, and global connectivity, AIBEDA transforms complex regulatory challenges into commercial success.
Are you passionate about clinical research and project management? Are you excited about medtech breakthroughs impacting people’s health? If the answers are yes, we want to hear from you.