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Senior Manager, Statistical Programming

Job in Freehold, Monmouth County, New Jersey, 07728, USA
Listing for: Autolus Limited
Full Time position
Listed on 2026-03-04
Job specializations:
  • Healthcare
    Data Scientist
Salary/Wage Range or Industry Benchmark: 80000 - 100000 USD Yearly USD 80000.00 100000.00 YEAR
Job Description & How to Apply Below
Senior Manager, Statistical Programming page is loaded## Senior Manager, Statistical Programming locations:
US-New Jersey (Remote) time type:
Full time posted on:
Posted Todaytime left to apply:
End Date:
May 15, 2026 (30+ days left to apply) job requisition :
JR100082
** Work with us
** Our team are passionate in the pursuit of excellence and in pushing the boundaries of cancer therapy and Autoimmune disease to deliver life-changing treatments to patients.

Whilst working at Autolus you will enjoy a flexible, diverse and dynamic working environment which actively promotes creativity, leadership and teamwork – together we are ONE Autolus.
*
* Job Description:

** Job Title :
Senior Manager, Statistical Programming

Reports to:

Senior Director, Statistical Data Department:
Biometrics

Hours:

40

Location:

US – Rockville
** About Autolus
** Autolus is a clinical-stage biopharmaceutical company developing next-generation, programmed T cell therapies for the treatment of cancer. Using a broad suite of proprietary and modular T cell programming technologies. The company is engineering precisely targeted, controlled and highly active T cell therapies that are designed to better recognise cancer cells, break down their defence mechanisms and eliminate these cells. Autolus has a pipeline of product candidates in development for the treatment of haematological malignancies and solid tumours.

** Why Autolus
** Our team is passionate in the pursuit of excellence and in pushing the boundaries of cancer therapy to deliver life-changing treatments to patients. Whilst working at Autolus you will enjoy a flexible, diverse, and dynamic working environment which actively promotes creativity, leadership and teamwork. In addition to this Autolus is proud to offer a competitive salary, performance related bonus as well as private medical insurance, life assurance, pension and access to an employee share scheme.

Autolus promotes flexible working.
** Our Promise
** Autolus is developing complex, breakthrough therapies for a globally diverse market and equally recognises that diversity amongst our people is critical to our mission. As we draw on our differences, what we’ve experienced, and how we work, we celebrate diversity and are committed to creating an inclusive environment for all employees
** Role Summary
** A Sr. Statistical Programming Manager provides timely support to the project team on all programming matters according to the project strategies. As an integral part of a project team, the incumbent provides project leadership and contributes to the programming support for processing data from clinical studies. Project requirements will be identified according to a Statistical Analysis Plan, programming specifications or user requirements/design documents using internal standards and guidelines.

The incumbent is responsible for leading the programming aspect of the project, both internally or CROs, for all programming deliverables and participates in the identification and development of programming standards and macro development to facilitate the creation of statistical deliverables from a single study through to regulatory approval, product launch, and annual reports. May be asked to oversee special projects / work with clinical task force.

Meets statistical ad-hoc requests of senior management.
** Key Responsibilities
*** Independently coordinate and oversee the preparation, execution, reporting and documentation of clinical project programming activities.  Provide programming input to CRF, SAP, data specifications, and tables, figures, and listings (TFLs) shells.
* Write SAS programs to generate derived analysis datasets, perform analysis, and TFLs.
* Perform ad-hoc flexible and rapid programming arising from questions generated from planned analyses and results.
* Ensure consistency and adherence to standards.
* Work with external vendor (e.g., CROs) on programming deliveries.
* Provide input to the design of the clinical trial database for proper data capture and to ensure data quality.
* Convert, verify and integrate multiple sources of incoming data for the creation of analysis datasets.
* Provide programming support for the…
Position Requirements
10+ Years work experience
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