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Weekend Statistical Programmer Jobs in Virginia (NOW HIRING)

... statisticians and data management teams • Support regulatory submissions and audits Minimum ... programming experience in clinical research • Experience with CDISC standards Preferred ...

Bachelor's or Master's degree in Statistics or related field 5+ years of SAS programming experience in clinical research Experience with CDISC standards Preferred Qualifications: Experience ...

... statisticians and data management teams • Support regulatory submissions and audits Minimum ... programming experience in clinical research • Experience with CDISC standards Preferred ...

... engineers, and fellow data scientists to: - Analyze large-scale security data using statistical ... We don't like getting paged in the middle of the night or on the weekend, so we work to ensure that ...

In addition, there may be occasional weekend work required. The candidate MUST be a US citizen and ... Develop and implement statistical models, machine learning workflows, and geospatial analytics ...

In addition, there may be occasional weekend work required. The candidate MUST be a US citizen and ... Develop and implement statistical models, machine learning workflows, and geospatial analytics ...

In addition, there may be occasional weekend work required. The candidate MUST be a US citizen and ... Develop and implement statistical models, machine learning workflows, and geospatial analytics ...

Company Description Jr. SAS Programmer Location: Alexandria, VA One year long contract Pay rate: up ... Client will hire an entry level person with a math degree, or statistics, etc. Responsibilities ...

... occasional evening or weekend if required * Ability to communicate effectively and work ... Ability to use standard word processing & spreadsheet software for reports, graphics and statistics

... occasional evening or weekend if required * Ability to communicate effectively and work ... Ability to use standard word processing & spreadsheet software for reports, graphics and statistics

Work Hours & On Call • 3-4 days at Ashburn office. • Rotating on call coverage, evening/weekend ... algorithms, and statistics, including working with SQL • ≥1 year working experience in ...

Manufacturing support for process deployment or continuous improvement including night or weekend ... Development and Application of Statistical Process Control for new processes * Proficient in ...

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Weekend Statistical Programmer information

What is the difference between Weekend Statistical Programmer vs Full-Time Statistical Programmer?

AspectWeekend Statistical ProgrammerFull-Time Statistical Programmer
CredentialsBachelor's degree in Biostatistics, Statistics, or related field; often requires programming certificationsSame as weekend role, with additional experience preferred
Work EnvironmentPart-time, flexible hours, often remote or in clinical research settingsFull-time, standard office or remote work in pharmaceutical or biotech companies
Employer & Industry UsageUsed in clinical trials, research organizations, and CROs for flexible staffingCommon in pharmaceutical, biotech, and research institutions for ongoing project support

The main difference between a Weekend Statistical Programmer and a Full-Time Statistical Programmer lies in their work hours and commitment. Weekend roles typically involve part-time, flexible schedules focused on specific project needs, while full-time roles require consistent, ongoing work. Both roles require similar skills and credentials, but the work environment and hours differ to accommodate project demands and work-life balance.

What are the most commonly searched types of Statistical Programmer jobs in Virginia? The most popular types of Statistical Programmer jobs in Virginia are:
What cities in Virginia are hiring for Weekend Statistical Programmer jobs? Cities in Virginia with the most Weekend Statistical Programmer job openings:

Biostatistical Prograrmming Manager

Amgen

Virginia Beach, VA • On-site

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

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Salary Range

129,056.35USD -174,605.65USD