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Cytel · 2 days ago
Senior Statistical Programmer
United States
Full-time
Hybrid
Senior Level
5+ years exp
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Responsibilities
Working under the direction of the Team Lead / Project Manager, the senior statistical programmer conducts programming activities for a trial, early phase project, indication, or publication activities.
Lead at least one study team in terms of providing technical and domain-related guidance.
May required to lead and manage a team of 2-4 members
Experience of working on Oncology TA is mandatory.
Ability to work on data migration from legacy datasets to standards such as CDISC or any other client-specific standard.
Read and understand the program specifications document.
Prepare SAS analysis datasets, tables, listings, and figures as per specifications.
Create programs to create graphs and tables that are required in CSRs, safety reports, efficacy reports, etc. ensuring on-time quality delivery.
Validate and transform datasets as per client assignment specifications.
Validate tables, listings, and figures as per client assignment specifications.
Coordinate with the client and US team for clarity of specifications, data issues, outliers, reviews, schedules, etc.
Contribute in the organization’s recruitment process by identifying needs and required skill sets of resources and conducting interviews to hire appropriate resources.
Perform all the above tasks using standard operating procedures (SOPs) as defined in the Quality Management System or the respective client(s) as applicable
Qualification
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Required
BS or MS degree in Computer Science, Statistics, or related health science field with a minimum of 5 years of SAS programming experience with clinical trial data
Experience of working on Oncology TA is mandatory
Ability to work on data migration from legacy datasets to standards such as CDISC or any other client-specific standard
Read and understand the program specifications document
Prepare SAS analysis datasets, tables, listings, and figures as per specifications
Create programs to create graphs and tables that are required in CSRs, safety reports, efficacy reports, etc. ensuring on-time quality delivery
Validate and transform datasets as per client assignment specifications
Validate tables, listings, and figures as per client assignment specifications
Coordinate with the client and US team for clarity of specifications, data issues, outliers, reviews, schedules, etc
Contribute in the organization’s recruitment process by identifying needs and required skill sets of resources and conducting interviews to hire appropriate resources
Perform all the above tasks using standard operating procedures (SOPs) as defined in the Quality Management System or the respective client(s) as applicable
Well-conversed with regulatory requirements and drug development process
Good understanding of the Clinical trial domain and good SAS programming skills
Ability to work independently
Company
Cytel
Cytel enables decision-makers in the life sciences to unlock the full potential of their products.
1,001-5,000 employees
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 StageTotal Funding
$2MKey Investors
New Mountain CapitalMerck Capital Ventures
2021-01-01Series Unknown· Undisclosed
2020-12-21Acquired· by Nordic Capital
2017-11-01Private Equity· Undisclosed
Leadership Team
Joshua Schultz
CEO
Cyrus Mehta
Co-Founder & President
Recent News
Company data provided by crunchbase
