At Cytel, we work hard to create successful careers with significant professional growth for our employees, as a result of which they work hard to make Cytel successful.
Cytel is a place where talent, experience and integrity come together to advance the state of clinical development.
Position is home:
based.
We are experiencing exponential growth on a global scale and hiring SeniorStatisticalProgrammers to join our FSP division.
You will apply your know:
how in CDISC standards (SDTM and ADaM) and advanced SAS programming skills, tosupport or lead one or more Phase I:
IV clinical trials, across a variety of therapeutic areas.
Our values
:
We believe in applyingscientific rigorto reveal the full promise inherent in data.
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We nurtureintellectual curiosityand encourage everyone to approach new challenges with enthusiasm and the desire for discovery.
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We believe incollaborationand invite a diversity of perspectives, drawing on a variety of talents to create a wealth of possibilities.
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We prizeinnovationand seek intelligent solutions using leading:
edge technology.
As a SeniorStatisticalProgrammer, you will leverage your advanced SAS programming skills and proficiency in CDISC standards (SDTM and 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:
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Performing data manipulation, analysis and reporting of clinical trial data, both safety and efficacy, utilizing SAS programming
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Generating and validating analysis datasets/analysis files, and complex tables, listings, and figures ( TLFs)
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Production and QC / validation programming
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Generating complex ad:
hoc reports utilizing raw data and analysis datasets
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Applying strong understanding/experience of Efficacy analysis
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Communicating with and/or responding to internal cross:
functional teams and client for project specifications, status, issues or inquiries
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Performing lead duties for assigned clinical study under principle programmers oversight
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Serving as team player, with a willingness to go the extra distance to get results, meet deadlines, etc.
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Being adaptable and flexible when priorities change
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Generating and validating Non:
CDISC transformation datasets and analysis datasets
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Proficient knowledge with SDTM/ADaM and TLF's.
General expertise with Figures
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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.
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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.
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R and complex macro writing are a plus
What you offer:
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Bachelor's degree in one of the following fieldsStatistics, Computer Science, Mathematics, etc.
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At least 8years of SAS programming working with clinical trial data in the Pharmaceutical and Biotech industrywith a bachelor's degree or equivalent.
At least 6years of related experience with a master's degree or above.
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Study lead experience, preferably juggling multiple projects simultaneously.
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Strong SAS data manipulation, analysis and reporting skills.
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Strong QC / validation skills.
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Good ad:
hoc reporting skills.
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Solid ADaM and complex TFL skills.
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Proficiency in efficacy analysis and survival analysis
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Familiarity with drug development life cycle and experience with the manipulation, analysis and reporting of clinical trials' data.
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Submissions experience utilizing define.xml and other submission documents
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Excellent analytical and troubleshooting skills.
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Ability to provide quality output and deliverables, in adherence with challenging timelines.
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Ability to work effectively and successfully in a globally dispersed team environment with cross:
cultural partners.
Why Cytel? Information Technology, Manufacturing, Science CDI Competitive
