Clinical SAS Programmer
Clinical SAS Programmer
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Salary Not Disclosed
1 Vacancy
Job Description
Responsibilities:
- Providing statistical programming support to generate tables listings and figures for assigned projects.
- Demonstrating proficiency in CDISC SDTM and Adam to support various submission activities including IA CSR DSUR and publications.
- Overseeing all aspects of statistical programming working closely with statisticians to ensure timely and accurate delivery of statistical outputs.
- Creating detailed specifications for individual studies and comprehensive summaries.
- Directing and supervising CRO activities related to statistical programming including the creation and validation of SDTM and Adam datasets.
- Producing safety tables efficacy tables and lab shift tables in accordance with the SAP and mock layouts.
- Reviewing statistical analysis plans annotated CRFs and integrated summaries providing thoughtful feedback.
- Validating datasets and tables through double programming.
- Having a good understanding of oncology-specific domains is an advantage.
Requirements:
- A masters or bachelors degree (or equivalent qualification) in a relevant field.
- At least 5 years of solid experience in statistical programming with clinical trial data particularly using SAS software.
- A strong team player who is open to learning and adopting new methods and technologies contributing positively to team dynamics.
- A quick learner with a proven history of effective collaboration and teamwork.
- Exceptional communication skills both written and verbal.
- Demonstrated ability to multitask prioritize anticipate potential challenges and achieve goals within a multidisciplinary team environment.
- Prior experience in oncology and vendor management is highly preferred.
Additional Information :
All your information will be kept confidential according to EEO guidelines.
Remote Work :
No
Employment Type :
Contract
Employment Type
Contract
