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Gage R&R studies * Statistical Process Control * Actively participates in Crane Business System ... engineering, with prior relevant internship/co-op experience preferred. * Must demonstrate ...
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Interns will have daily programming responsibilities in R, Python, and SQL (project-specific). They ... statistics, or related field; * Analytical thinker with great attention to detail; * Ability to ...
Interns will have daily programming responsibilities in R, Python, and SQL (project-specific). They ... statistics, or related field; * Analytical thinker with great attention to detail; * Ability to ...
Interns will have daily programming responsibilities in R, Python, and SQL (project-specific). They ... statistics, or related field; * Analytical thinker with great attention to detail; * Ability to ...
Interns will have daily programming responsibilities in R, Python, and SQL (project-specific). They ... statistics, or related field; * Analytical thinker with great attention to detail; * Ability to ...
Interns will have daily programming responsibilities in R, Python, and SQL (project-specific). They ... statistics, or related field; * Analytical thinker with great attention to detail; * Ability to ...
Internship R Statistical Programmer information
What is the difference between Internship R Statistical Programmer vs R Statistical Programmer?
| Aspect | Internship R Statistical Programmer | R Statistical Programmer |
|---|---|---|
| Required Credentials | Typically pursuing or recently completed a degree in statistics, biostatistics, or related field | Bachelor's or master's degree in statistics, biostatistics, or related field; professional experience preferred |
| Work Environment | Internship setting, often part-time or temporary, supervised by senior staff | Full-time, permanent role within pharmaceutical, biotech, or healthcare industries |
| Employer & Industry Usage | Used in academic, research, or entry-level industry settings | Common in clinical research, pharmaceutical companies, and CROs |
The main difference between an Internship R Statistical Programmer and an R Statistical Programmer is experience level and employment status. Internships are typically temporary positions for students or recent graduates gaining practical experience, while R Statistical Programmers are full-time professionals responsible for developing and maintaining statistical programming in clinical trials or research projects.
What are the key skills and qualifications needed to thrive as an Internship R Statistical Programmer, and why are they important?
What does an Internship R Statistical Programmer do?
What does a typical day look like for an Internship R Statistical Programmer, and how do interns collaborate with other team members?
Full-time
Posted 4 days ago
Job 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