Job Summary :
We are seeking an experienced Statistical Programmer to join our team. The successful candidate will be responsible for performing consistency reviews of clinical trial documents, authoring and reviewing study TFL shells and dataset standards, programming and QC routine and ad hoc datasets and TFLs in SAS, completing and reviewing CDISC Validation tool reports, evaluating data using frequencies, histograms, t-test, ANOVA, regression, standard survival techniques, and reviewing project management related documents.
Key Responsibilities :
- Consistency Review : Perform thorough reviews of clinical trial documents to ensure accuracy and completeness.
- TFL Programming : Author and review study TFL shells and dataset standards, program and QC routine and ad hoc datasets and TFLs in SAS.
- Data Analysis : Evaluate data using frequencies, histograms, t-test, ANOVA, regression, standard survival techniques.
- CDISC Reporting : Complete and review CDISC Validation tool reports.
Requirements :
Oncology Experience : A minimum of 2 years of experience in oncology.R Programming Skills : Advanced R programming skills, with experience in ADaM / TLF programming.Agile Mindset : Affinity for agile ways of working.Preferred Skills :
Advanced R Programming : Expert level R programming skills.ISS / ISE / Submissions / RTQs Experience : Experience in ISS / ISE / Submissions / RTQs.