Job Highlights
Not Disclosed
Posted 1 year ago
Job details
职位来源于智联招聘。
岗位职责:
Able to conduct programming daily works independently, including generate TFLs, SDTM/ADaM mapping and specification development, QC and documentation, etc.
Write, modify, and maintain SAS programs for the creation of ADS and TFLs in an efficient manner.
Perform program validation and quality control of ADS and TFLs produced by other programmer.
Identify the programming issues and fill the issue and action tracking log where applicable.
Update the programming quality control record with programming or QC details.
Provide programming support for data management and data validation as needed.
Understand, execute and improve company SAS macros.
Produce the derived dataset specifications, programming specifications, and other process supporting documents.
Learn internal and external SOPs/WPDs, ICH-GCP and/or other international/local regulatory requirements.
Ensure all statistical activities in accordance with internal and external quality standards, SOPs/WPDs, ICH-GCP and/or other international/local regulatory requirements.
Improve technical skills including SAS programming, statistics and clinical trial through self-learning, coaching, internal training, external training, and on-job training, etc.
Develop effective team communication and team work.
Proactively participate in process/quality improvement initiatives.
任职要求:
At least 2 years full time work experience as SAS programmer thoroughly supporting clinical trial.
Bachelor degree or above
Familiar with CDISC.
Nice to familiar with R, python, etc
Experience in Oncology is desirable
Have good capability in self-learning, communication and planning.
Better to have experience in global pharmaceutical company studies
Better to have strategic thinking and risk management sense.
Be capable of working under high pressure
Requirement on EN
Listening-able to take EN training and meetings
Speaking-able to communicate with EN speaking people clearly
Reading-able to read EN protocol and academic materials
Writing-able to write EN e-mails and reports
职位福利:股票期权、五险一金、交通补助、餐补、通讯补助、带薪年假、补充医疗保险、定期体检
以担保或任何理由索要财物,扣押证照,均涉嫌违法。
岗位职责:
Able to conduct programming daily works independently, including generate TFLs, SDTM/ADaM mapping and specification development, QC and documentation, etc.
Write, modify, and maintain SAS programs for the creation of ADS and TFLs in an efficient manner.
Perform program validation and quality control of ADS and TFLs produced by other programmer.
Identify the programming issues and fill the issue and action tracking log where applicable.
Update the programming quality control record with programming or QC details.
Provide programming support for data management and data validation as needed.
Understand, execute and improve company SAS macros.
Produce the derived dataset specifications, programming specifications, and other process supporting documents.
Learn internal and external SOPs/WPDs, ICH-GCP and/or other international/local regulatory requirements.
Ensure all statistical activities in accordance with internal and external quality standards, SOPs/WPDs, ICH-GCP and/or other international/local regulatory requirements.
Improve technical skills including SAS programming, statistics and clinical trial through self-learning, coaching, internal training, external training, and on-job training, etc.
Develop effective team communication and team work.
Proactively participate in process/quality improvement initiatives.
任职要求:
At least 2 years full time work experience as SAS programmer thoroughly supporting clinical trial.
Bachelor degree or above
Familiar with CDISC.
Nice to familiar with R, python, etc
Experience in Oncology is desirable
Have good capability in self-learning, communication and planning.
Better to have experience in global pharmaceutical company studies
Better to have strategic thinking and risk management sense.
Be capable of working under high pressure
Requirement on EN
Listening-able to take EN training and meetings
Speaking-able to communicate with EN speaking people clearly
Reading-able to read EN protocol and academic materials
Writing-able to write EN e-mails and reports
职位福利:股票期权、五险一金、交通补助、餐补、通讯补助、带薪年假、补充医疗保险、定期体检
以担保或任何理由索要财物,扣押证照,均涉嫌违法。
Benefits Offered?
- No
Bonus Offered?
- No
Travel Required?
- No
Location:
- China
Global Experience Needed?
- No
Specialized Experience Needed?
- No
Apply before:
- Apr 15, 2024
Company Overview

杭州泰格医药科技股份有限公司
Current Openings: 0
杭州泰格医药科技股份有限公司 is an information technology and services company based out of 浙江省杭州市滨江区江南大道618号东冠大厦1502-1室, 杭州市, 浙江省, China.
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