Similar posts
Senior SAS Programmer
- Permanent
- Statistics
- United Kingdom
This vacancy has now expired. Please see similar roles below...
ProClinical is happy to advertise new a UK home-based Senior SAS Programmer role for one of the largest pharmaceutical organisations in the market. This position will focus on developing statistical methods effectively optimising the company.
Job Responsibilities
- Develop SAS programs for generating datasets, tables, figures and listings for clinical trials (according to ICH E3) and/or publication and/or Health Authorities requests
- Be the CDISC SDTM/ADaM expert; use CDISC guidelines to generate SDTM/ADaM datasets
- Develop standard SAS macros and prepare the corresponding validation documents
- Perform quality check on SAS programs/outputs created by another Statistician/SAS Programmer
- Develop SAS programs/macros and utilities for data cleaning
- Liaise with Data Management team in identifying and implementing checks according to the Data Validation Plan
- Check the requirements to handle external clinical data and develop the SAS programs to import/reconcile external clinical data
- Develop and validate SAS programs for identification of Protocol Deviations
- Establish and implement programming rules
- Collaborate with Biostatistics and Data Management staff on clinical trials/projects
- Prepare, maintain, and archive of SAS programming documentation
- Collaborate in establishing and maintaining SOPs related to SAS programming
- Collaborate in establishing and maintaining document/programming standards
- Contribute to on-boarding of new associates and act as a mentor for junior staff
- Keep informed on new SAS developments relevant to the clinical trial data management
Skills and Requirements
- Educated to degree level in a relevant discipline and/or equivalent work experience.
- Proficiency in SAS.
- Extensive knowledge and understanding of the programming and reporting process.
- Knowledge of SOP's/Guidelines, ICH-GCP, and any other applicable local and international regulations such as 21 CFR Part 11.
- Ability to learn new systems and function in an evolving technical environment.
- Strong project management skills.
- Ability to successfully lead a global team with proven Lead programming experience.
- Competent in written and oral English.
To Apply
ProClinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.
#LI-SB1
#Biometrics
Related jobs
US$205000 - US$214000 per annum
Washington Grove, USA
Ready to shape the future of clinical statistics? Step into a pivotal leadership role as Director of Biostatistics with one of our forward-thinking clients.
Highly Competitive
London, England
Proclinical is seeking a Lead Biostatistician with a focus on oncology to permanently join our client's team.
US$190000 - US$220000 per annum
San Francisco, USA
Ready to revolutionize biotech? Join a rising force that's redefining the future of healthcare and science!
US$200000 - US$220000 per annum
San Francisco, USA
Are you ready to make a groundbreaking impact in the world of biotechnology? Join a growing company that's shaping the future of healthcare and science.
Highly Competitive
Boston, USA
Proclinical is partnering with an innovative biotech company to recruit a Director of Biostatistics.