location_onLondon, UK
watch_later Posted: Apr 11, 2024
Skills Required
Nice To Have skills
Job Description
As a Senior Statistical Programmer, you will leverage your advanced SAS programming skills and proficiency in CDISC standards (SDTM ADaM) to support or lead one or more Phase I-IV clinical trials. This role can be performed as fully remote.
How you will contribute:
- Performing data manipulation, analysis and reporting of clinical trial data, both safety and efficacy, utilizing SAS programming
- Generating and validating analysis datasets/analysis files, and complex tables, listings, and figures ( TLFs)
- Production and QC / validation programming
- Generating complex ad-hoc reports utilizing raw data and analysis datasets
- Applying strong understanding/experience of Efficacy analysis
- Communicating with and/or responding to internal cross-functional teams and client for project specifications, status, issues or inquiries
- Performing lead duties for assigned clinical study under principle programmers oversight
- Serving as team player, with a willingness to go the extra distance to get results, meet deadlines, etc.
- Being adaptable and flexible when priorities change
- Generating and validating Non-CDISC transformation datasets and analysis datasets
- Proficient knowledge with SDTM/ADaM and TLF’s. General expertise with Figures
- Individuals should be able to start programs from scratch and have the ability to handle complicated domains and outputs related to the protocol and SAP.
- They must demonstrate a good understanding of the endpoints and data collection, with the ability to read and write specifications related to the respective implementation guides.
- R complex macro writing are a plus
What you offer:
- Bachelor’s degree in one of the following fields Statistics, Computer Science, Mathematics, etc.
- At least 8 years of SAS programming working with clinical trial data in the Pharmaceutical Biotech industry with a bachelor’s degree or equivalent. At least 6 years of related experience with a master’s degree or above.
- Study lead experience, preferably juggling multiple projects simultaneously.
- Strong SAS data manipulation, analysis and reporting skills.
- Strong QC / validation skills.
- Good ad-hoc reporting skills.
- Solid ADaM and complex TFL skills.
- Proficiency in efficacy analysis and survival analysis
- Familiarity with drug development life cycle and experience with the manipulation, analysis and reporting of clinical trials’ data.
- Submissions experience utilizing define.xml and other submission documents
- Excellent analytical troubleshooting skills.
- Ability to provide quality output and deliverables, in adherence with challenging timelines.
- Ability to work effectively and successfully in a globally dispersed team environment with cross-cultural partners.