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Assistant R Statistical Programmer Jobs in Indiana

... results, assist/respond to regulatory queries. * Assist in and/or be accountable for selecting ... Maintain proficiency with respect to SAS/R programming and statistical methodology and in applying ...

Student (1)

West Lafayette, IN · On-site

$14.75 - $18.50/hr

Student (1) City: West Lafayette Job Summary Seeking a motivated student assistant to support a ... Proficiency with R statistical software * Basic understanding of statistical methods Experience 0 ...

Our experienced statisticians and programmers develop intellectual property and assets to support ... Experience in SAS and/ or R statistical software packages. * Experience in study design and ...

Collaborate with team members to write reports and communicate results. * Assist with, or be ... Proficient in statistical programming languages/software such as SAS, R, Spotfire, etc

... results, assist/respond to regulatory queries. * Assist in and/or be accountable for selecting ... Proficiency in statistical programming languages/software such as SAS, R, Spotfire, etc.

Sr. Advisor - Statistics

Indianapolis, IN · On-site

$83K - $102K/yr

Collaborate with team members to write reports and communicate results. * Assist with, or be ... Proficient in statistical programming languages/software such as SAS, R, Spotfire, WinBUGs, etc

CNC MFG Engineer

Warsaw, IN · On-site

$70K - $89K/yr

Job Title: Sr CNC MFG Engineer Location: Warsaw, IN JD as below * Role: Validate CNC equipment and ... Analyze process data (statistical methods, capability studies like Cp/Cpk, Gage R&R) to demonstrate ...

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Assistant R Statistical Programmer information

What is the difference between Assistant R Statistical Programmer vs Data Analyst?

AspectAssistant R Statistical ProgrammerData Analyst
Required SkillsProficiency in R, basic statistical knowledge, programming skillsData manipulation, visualization, statistical analysis, often using R or Excel
Work EnvironmentClinical research, pharmaceutical, or biotech industriesBusiness, marketing, finance, healthcare sectors
CertificationsOften requires a degree in statistics, biostatistics, or related fieldsDegree in statistics, data science, or related fields; certifications like CAP or Microsoft certifications are common

While both roles involve data analysis and programming skills, the Assistant R Statistical Programmer primarily supports clinical trials and pharmaceutical research, focusing on statistical programming in R. Data Analysts work across various industries analyzing data to inform business decisions. The roles share similar educational backgrounds but differ in industry focus and specific job functions.

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What job categories do people searching Assistant R Statistical Programmer jobs in Indiana look for? The top searched job categories for Assistant R Statistical Programmer jobs in Indiana are:
What cities in Indiana are hiring for Assistant R Statistical Programmer jobs? Cities in Indiana with the most Assistant R Statistical Programmer job openings:
Infographic showing various Assistant R Statistical Programmer job openings in Indiana as of June 2026, with employment types broken down into 76% Full Time, 17% Part Time, and 7% Contract. Highlights an 83% Physical, 4% Hybrid, and 13% Remote job distribution.

Biostatistical Prograrmming Manager

Amgen

Indianapolis, IN

Full-time

Posted 2 days ago


Job description

Career CategoryClinicalJob Description

Biostatistical Programming Manager

What you will do

Let's do this. Let's change the world. In this vital role you will provide both strategic oversight and hands-on statistical programming support to enable high-quality and timely clinical trial deliverables.

This role is part of the centrally managed Quality and Quick Response (QQR) Programming team and is responsible for supporting urgent and high-priority programming needs across development programs. The manager will serve as a technical programming expert who can rapidly respond to internal and external requests, support special projects, provide global quality oversight, and contribute directly to programming deliverables when needed.

This role will primarily support programs within the Obesity Therapeutic Area and requires close collaboration with cross-functional teams to support fast-paced development activities and evolving business priorities.

Responsibilities

Provide rapid response statistical programming support for urgent internal and external requests

Serve as a lead programmer for studies and projects, such as Data Access Plan (DAP) activities, unblinding efforts, and special projects

Deliver hands-on programming support for SDTM, ADaM, Tables, Listings, and Figures (TFLs), and other study and regulatory submission deliverables as needed

Oversee the execution and quality of projects managed by our FSP partners per Amgen Global Statistical Programming (GSP) Quality Oversight Plan (QOP)

Ensure that FSP and in-house programming deliverables meet quality, compliance, timeline, and productivity expectations

Mitigate at-risk projects by providing technical expertise, programming support, and operational guidance

Contribute to training material development and delivery to internal teams and FSP partners

Provide guidance and technical consultancy to study programming team on Amgen processes, tools, and utilities

Lead/contribute to GSP continuous improvement iniatives and support cross-functional initiatives including inspection readiness, process improvement, innovation, and training activities

Contribute to programming team performance metrics development, data collection, and reporting

Review project documentation such as specifications, issue logs, deliverable status for accuracy and completeness

What we expect of you

We are all different, yet we all use our unique contributions to serve patients. The dynamic professional we seek is a manager with these qualifications.

Basic Qualifications:

Doctorate degree OR

Master's degree and 2 years of statistical programming experience OR

Bachelor's degree and 4 years of statistical programming experience OR

Associate's degree and 8 years of statistical programming experience OR

High school diploma / GED and 10 years of statistical programming experience

Preferred Qualifications:

Masters in Computer Science, Statistics, Mathematics, Computer Science, Life Sciences or another relevant scientific subject

6+ years of statistical programming in biopharmaceutical industry

Regulatory submission experience

Strong hands-on SAS programming expertise including SAS Base, Macro, SQL, SAS/Graph and Stat packages

Experience with R programming for clinical trial analyses, data manipulation, reporting and visualization preferred

Familiarity with additional programming languages and tools such as Python preferred

Hands-on experience developing and validating SDTM, ADaM datasets, and TFLs

Thorough understanding of clinical trial processes from data collection through analysis and reporting

Ability to lead programmers in successful completion of all study programming activities and provide guidance on technical and process questions

Strong understanding of data standards and compliance checks including Pinnacle 21

Experience providing quality oversight for outsourced and internal programming deliverables

Ability to troubleshoot complex technical issues and turnaround at-risk projects

Experience working in a globally dispersed team on Phase 1-4 clinical trials

Experience supporting clinical development programs within the Obesity Therapeutic Area preferred

Understanding of obesity clinical endpoints, data standards, and regulatory considerations is highly desirable

Excellent oral and written English communication skills; strong collaboration, negotiation, and organizational skills

.

Salary Range

129,056.35USD -174,605.65USD