Principal Statistical Programmer @ Cytel | Jobright.ai
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Cytel · 2 days ago

Principal Statistical Programmer

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Responsibilities

Performing data manipulation, analysis, and reporting of clinical trial data using SAS programming
Generating and validating SDTM and ADaM datasets/analysis files, and tables, listings, and figures (TLFs)
Production and QC/validation programming
Programming from scratch and handling complicated domains and TLFs
Reading and applying protocol and SAP
Demonstrating good understanding of endpoints and data collection
Generating complex ad-hoc reports from raw data
Applying strong experience in Efficacy analysis
Creating and reviewing submission documents and eCRTs
Communicating with internal cross-functional teams and clients for project specifications and status updates
Performing lead duties when required
Being adaptable and flexible when priorities change
Writing complex macros and having general expertise with Figures
Leading other programmers

Qualification

Find out how your skills align with this job's requirements. If anything seems off, you can easily click on the tags to select or unselect skills to reflect your actual expertise.

SAS Data ManipulationCDISC SDTM/ADaM StandardsQC/ValidationAd-Hoc ReportingEfficacy AnalysisDrug Development Life CycleClinical Trials Data AnalysisSubmissions Define.xmlQuality Output DeliveryProblem-SolvingAnalyticalTroubleshootingEffective CommunicationTime ManagementTeamworkRare DiseasesGastrointestinal Studies

Required

Bachelor’s degree in one of the following fields Statistics, Computer Science, Mathematics, or related field
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 preferred.
Strong SAS data manipulation, analysis, and reporting skills.
Solid experience implementing the latest CDISC SDTM / ADaM standards.
Strong QC / validation skills.
Good ad-hoc reporting skills.
Proficiency in Efficacy 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.

Preferred

Experience supporting Rare Diseases and Gastrointestinal studies would be a plus.

Benefits

Competitive compensation
Excellent benefits package
Annual bonus incentive
Work-life balance

Company

Cytel enables decision-makers in the life sciences to unlock the full potential of their products.

H1B Sponsorship

Cytel has a track record of offering H1B sponsorships. Please note that this does not guarantee sponsorship for this specific role. Below presents additional info for your reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Trends of Total Sponsorships
2023 (30)
2022 (48)
2021 (38)
2020 (36)

Funding

Current Stage
Late Stage
Total Funding
$2M
Key Investors
New Mountain CapitalMerck Capital Ventures
2021-01-01Series Unknown· Undisclosed
2020-12-21Acquired· by Nordic Capital
2017-11-01Private Equity· Undisclosed

Leadership Team

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Joshua Schultz
CEO
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Cyrus Mehta
Co-Founder & President
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Company data provided by crunchbase
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