Scientist, Statistical Programming Position Available In Union, New Jersey

Scientist, Statistical Programming
Scientist, Statistical Programming
remote type
Not Applicable
locations
USA – New Jersey – Rahway
time type
Full time
posted on
Posted 6 Days Ago
time left to apply

End Date:

August 31, 2025 (30+ days left to apply)
job requisition id
R344769
Job Description
Responsibilities
Support statistical programming analysis and reporting deliverables for global PK modeling and simulation stakeholders spanning all therapeutic areas.
Develop and execute modeling-ready analysis and reporting datasets, tables, listings, figures and submission deliverables under the guidance of a senior level programmer.
Perform validation tasks according to departmental SOPs and collaborate effectively with outsource partners.
Act as a key collaborator with modelers, statisticians, and other project stakeholders to gather and document user requirements for statistical programming deliverables.
Programmatically synthesize preclinical data into analysis ready structures from varied data sources.
Programmatically develop, validate and maintain modeling-ready datasets by integrating PK, PD and covariate data.
Produce tables and graphics for inclusion in study reports and regulatory submissions.
Produce SAS transport files and associated documentation for regulatory submissions.
Assure deliverable quality andpliance with departmental SOPs and good programming practices.
Collaborate effectively with project team members including outsource provider staff.
Minimum educational requirement
Must have a Master’s degree in Computer Science, Statistics, Applied Mathematics, Life Sciences, Engineering or related field OR a Bachelor’s degree in Computer Science, Statistics, Applied Mathematics, Life Sciences, Engineering or related field plus at least 2 years SAS programming experience in a clinical trial environment.
Required experience and skills
Must possess SAS programming skills including data steps, procedures, SAS/MACRO, SAS/GRAPH.
Knowledge and skills in developing analysis and reporting deliverables for R D projects (data, analyses, tables, graphics, listings); knowledge of pharmaceutical development processes; and knowledge in CDISC SDTM and ADaM standards required.
Must possess abilities to quickly and effectively learn new program techniques and data structures; to take direction effectively andplete programming tasks under the guidance of a senior programmer at a project level; and to collaborate with key stakeholders.
Must have an interest and ability to work in an exploratory environment, handling non-standard data in a variety of formats with minimal requirements; and an interest to advance career by investing in development activities and taking on tasks with increasing levels of challenge and responsibility.
Good interpersonal skills and ability to negotiate and collaborate effectively; good written, oral, and presentation skills also required.
The salary range for this role is
$94,300.00 to $148,500.00
This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this posting. An employee’s position within the salary range will be based on several factors including, but not limited to relevant education, qualifications, certifications, experience, skills, geographic location, government requirements, and business or organizational needs.
The successful candidate will be eligible for annual bonus and long-term incentive, if applicable.
We offer aprehensive package of benefits. Available benefits include medical, dental, vision healthcare and other insurance benefits (for employee and family), retirement benefits, including 401(k), paid holidays, vacation, andpassionate and sick days. More information about benefits is available at Compensation and Benefits Webpage.
You can for this role through the Career Site (or via the Workday Jobs Hub if you are a current employee). The application deadline for this position is stated on this posting.