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Senior Statistical Programmer

Orchard Therapeutics - U.S.

London

On-site

GBP 50,000 - 80,000

Full time

6 days ago

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Job summary

A leading company in transformative gene therapies seeks a Senior Statistical Programmer in London to enhance its Biostatistics team. This hands-on role requires expert SAS programming skills and adherence to CDISC standards for data management. The position promises valuable contributions to clinical drug development projects, with a collaborative team environment and multiple project involvement.

Qualifications

3+ years in clinical trial SAS programming.
Knowledge of CDISC standards required.
Experience with SAS GRAPH and SAS ODS preferred.

Responsibilities

Write SAS programs for analysis datasets, tables, listings, figures.
Adhere to CDISC standards for data management.
Deliver regulatory and publication outputs to agreed timelines.

Skills

SAS programming

CDISC standards

Attention to detail

Communication skills

Cross-functional collaboration

Education

BSc in mathematics, statistics, computer science or related discipline

1 day ago Be among the first 25 applicants

Location: London

Reporting to: Executive Director Biostatistics

The Senior Statistical Programmer at Orchard Therapeutics is a key member of a Biostatistics team working to provide transformative gene therapies to patients. Reporting to the Executive Director Biostatistics, this role provides a unique opportunity to use your programming skills in the production of data analyses from all phases of clinical drug development.

Key Elements And Responsibilities

In this role you will be expected to perform programming activities across multiple studies or projects to deliver datasets and statistical outputs to agreed timelines and quality. This will be a hands-on role in which you will be expected to produce both datasets and outputs.

Key Responsibilities Will Include

Writing SAS programs to create analysis datasets, tables, listings, and figures.
Adhere to CDISC standards for data management and analysis, including SDTM (Study Data Tabulation Model) and ADaM (ADAM Data Model).
Deliver all required outputs to agreed timelines and quality, (e.g., analysis datasets, pooled datasets, tables, figures and listings for regulatory or reimbursement submissions and publications).
Participate in the design and/or review of statistical programming deliverables including developing programming specifications for datasets and data outputs.
Participate in the review of other biometrics deliverables (e.g., case report forms, study database structure, data management and data quality plans, statistical analysis plans).
Oversight of statistical programming tasks outsourced to CROs, ensuring that their performance meets the agreed quality.

Requirements

Required Knowledge

3+ years of experience in clinical trial SAS programming.
Demonstrated knowledge of and experience in applying CDISC standards.
Self-starter with the ability to work within a Biostatistics team.

Skills And Abilities

Proficiency with SAS programming and SAS macro code development required along with a good understanding of SAS GRAPH and SAS ODS.
Understanding of clinical trial data and terminology.
Strong attention to detail and accuracy.
Excellent written and verbal communication skills.
Experience working with cross-functional groups.
Ability to manage multiple priorities and work effectively under pressure.
Knowledge of R would be an advantage.

Education

BSc or higher in mathematics, statistics, computer science or related discipline.

Seniority level

Seniority level
Associate

Employment type

Employment type
Full-time

Job function

Job function
Other

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