Company:
Katalyst Healthcares & Life Sciences
Location: Somerset
Closing Date: 20/10/2024
Hours: Full Time
Type: Permanent
Job Requirements / Description
Responsibilities:
Overseeing SAS programming activities from varying aspects: programming, statistical and clinical.
Create, manage, and maintain the SAS programming algorithm for the clinical study database and data analysis.
Peer reviews the submission packages and contribute to the input of SAP and mock TFLs.
Perform ad hoc analyses to support Phase I to IV clinical trials and medical publications.
Maintain relationships with internal and external customers and vendors
Mentor up and coming junior programmers and analysts.
Tracking projects against goals and submit status reports to project management.
Requirements:
Bachelor's or advanced degree in statistics, biostatistics, computer science or related fields.
4 to 6 years' experience in the pharma/biotech industry.
Advanced SAS programming skills (e.g, SAS SQL, SAS Macro, SAS/STAT, SAS/GRAPH, etc.) with clinical trial data.
Advanced knowledge in industry standards, such as the ICH guidelines, CDISC standards, 21 CFR Part 11, and FDA guidelines.
Experience in handling and processing upstream data, e.g., EDC, eDT, SDTM, and in providing outputs to meet downstream requirements, e.g., ADaM, define.xml and TFLs.
Overseeing SAS programming activities from varying aspects: programming, statistical and clinical.
Create, manage, and maintain the SAS programming algorithm for the clinical study database and data analysis.
Peer reviews the submission packages and contribute to the input of SAP and mock TFLs.
Perform ad hoc analyses to support Phase I to IV clinical trials and medical publications.
Maintain relationships with internal and external customers and vendors
Mentor up and coming junior programmers and analysts.
Tracking projects against goals and submit status reports to project management.
Requirements:
Bachelor's or advanced degree in statistics, biostatistics, computer science or related fields.
4 to 6 years' experience in the pharma/biotech industry.
Advanced SAS programming skills (e.g, SAS SQL, SAS Macro, SAS/STAT, SAS/GRAPH, etc.) with clinical trial data.
Advanced knowledge in industry standards, such as the ICH guidelines, CDISC standards, 21 CFR Part 11, and FDA guidelines.
Experience in handling and processing upstream data, e.g., EDC, eDT, SDTM, and in providing outputs to meet downstream requirements, e.g., ADaM, define.xml and TFLs.
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