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Intern Principal Statistical Programmer Jobs in Suwanee, GA

ACS REAL Intern

Atlanta, GA · On-site +1

$16 - $21/hr

The Research Intern will work with investigators on cancer prevention, cancer survivorship, health ... Strong Stata programming (or other statistical software) skills. Preferred Medical Expenditure ...

Lab Intern

Atlanta, GA · On-site

$14.50 - $19.25/hr

Qualifications Those who have completed statistical coursework and at least 2 chemistry laboratory ... Chemistry, Chemical Engineering and Materials Sciences majors are preferred, but others will be ...

Lab Intern

Atlanta, GA · On-site

$14.50 - $19.25/hr

Qualifications Those who have completed statistical coursework and at least 2 chemistry laboratory ... Chemistry, Chemical Engineering and Materials Sciences majors are preferred, but others will be ...

... experience of app developers and users. As Slack builds out its next generation of Platform ... statistical methods, experimentation, segmentation frameworks, and forecasting methodologies to ...

New

... experience of app developers and users. As Slack builds out its next generation of Platform ... statistical methods, experimentation, segmentation frameworks, and forecasting methodologies to ...

New

Networks - Initiates and maintains extensive contacts with transportation planning, engineering ... S. Census Bureau, and the Bureau of Transportation Statistics (BTS). * Experience developing ...

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Showing results 1-20

Intern Principal Statistical Programmer information

See Suwanee, GA salary details

$51

$78

$108

How much do intern principal statistical programmer jobs pay per hour?

As of Aug 27, 2026, the average hourly pay for intern principal statistical programmer in Suwanee, GA is $78.70, according to ZipRecruiter salary data. Most workers in this role earn between $67.79 and $90.82 per hour, depending on experience, location, and employer.

What does an intern principal statistical programmer do?

An Intern Principal Statistical Programmer assists in developing, validating, and implementing complex statistical programs used in the analysis of clinical trial data. They work under the guidance of senior programmers to perform data manipulation, statistical analysis, and generate summary reports or tables for regulatory submissions. Their role often involves learning industry standards, working with statistical software such as SAS or R, and collaborating with biostatisticians and data managers to ensure data quality and integrity.

What types of projects and responsibilities can an intern principal statistical programmer expect during their internship?

As an Intern Principal Statistical Programmer, you will typically assist with programming tasks related to clinical trial data analysis, such as developing and validating statistical programs using SAS or R. You'll often collaborate closely with statisticians and data managers to ensure data quality and regulatory compliance. Common responsibilities include generating tables, listings, and figures, supporting data cleaning activities, and learning about standard operating procedures. This role also offers exposure to cross-functional teamwork and opportunities to develop technical expertise in a real-world pharmaceutical or CRO environment.

What are the key skills and qualifications needed to thrive as an intern principal statistical programmer, and why are they important?

To thrive as an Intern Principal Statistical Programmer, you need a solid background in statistics, programming (especially in SAS or R), and a relevant degree such as statistics, mathematics, or computer science. Familiarity with clinical trial data standards (like CDISC), data management systems, and regulatory guidelines is typically required. Excellent problem-solving skills, attention to detail, and effective communication are crucial soft skills for success in this role. These competencies ensure accurate data analysis, regulatory compliance, and effective collaboration within multidisciplinary clinical research teams.

Senior Principal Programmer, Atlanta, GA

Atlanta, GA • On-site

UCB
Finance and Insurance • 1 - 5K employees

Full-time

Re-posted 6 days ago


Job description

Make your mark for patients
We are looking for a Senior Principal Programmer (Statistical Computing Environment Business Coordinator) who is collaborative, detail-oriented, and compliance-minded to join our Programming, Visualization and Reporting team, based inRaleigh, NC or Atlanta, GA.
About the role
You will help clinical programming teams move to and work confidently within UCB's modern Statistical Computing Environment. You will translate clinical reporting needs into well-governed study setups, support compliant platform operations, and help improve the way teams generate, validate, and deliver clinical trial analysis and reporting outputs.
Who you'll work with
You will work with the Programming, Visualization and Reporting team, statistical programming teams, platform administrators, Biometrics partners, and business stakeholders. You will connect technical and business needs, support users through onboarding and daily operations, and help teams follow consistent, compliant, and practical ways of working.
What you'll do
You will review and coordinate clinical trial analysis and reporting setup requests, making sure they are complete, accurate, and delivered on time.
You will configure study structures, repositories, datasets, reporting components, and access in line with CDISC and governance requirements.
You will manage role-based access, study configurations, and Git/Azure DevOps resources using approved requests and compliant processes.
You will coordinate environment provisioning with platform administrators so study teams can begin work in a ready and reliable environment.
You will support programming teams during onboarding, transition from legacy systems, and ongoing operations as a first-line technical contact.
You will improve lifecycle management and workflows by documenting processes, supporting validation activities, and automating practical solutions that enhance quality and user experience.
Interested? For this position you'll need the following education, experience and skills:
You bring 5+ years of experience in clinical trial results generation, reporting, and submission processes.
You have experience supporting Statistical Computing Environments, including process flows, user access, and Biometrics requirements.
You understand CDISC standards, including SDTM and ADaM, and have worked with Tables, Figures, and Listings.
You have worked in regulated pharmaceutical environments and understand SDLC, validation, audit readiness, and compliant configuration expectations.
You can communicate clearly with technical teams and business stakeholders, while tracking setup processes across systems and teams.
You bring practical experience with tools such as Domino Data Lab, SAS, R, Git, Azure DevOps, VS Code, or SAS Studio.
Are you ready to 'go beyond' to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!
About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.
Why work with us?
At UCB, we don't just complete tasks, we create value. We aren't afraid to push forward, collaborate, and innovate to make our mark for patients. We have a caring, supportive culture where everyone feels included, respected, and has equal opportunities to do their best work. We 'go beyond' to create value for our patients, and always with a human focus, whether that's on our patients, our employees, or our planet. Working for us, you will discover a place where you can grow, and have the freedom to carve your own career path to achieve your full potential.
At UCB, we've embraced a hybrid-first approach to work, bringing teams together in local hubs to foster collaborative curiosity. Unless explicitly stated in the description or precluded by the nature of the position, roles are hybrid with 40% of your time spent in the office.
UCB is an equal opportunity employer. All employment decisions will be made without regard to any characteristic protected by applicable federal, state, or local law. UCB invites you to voluntarily self-identify during the application process. Provision of self-identification information is entirely voluntary and a decision to provide or not provide such information will not have any effect on your application for employment, your employment with UCB, or otherwise subject you to any adverse treatment. Any information you provide will be considered confidential and will be kept separate from your application and/or personnel file and will only be used in accordance with applicable laws, orders, and regulations.
Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities contact us on US-Reasonable_Accommodation@ucb.com for application to US based roles. Please note should your enquiry not relate to adjustments; we will not be able to support you through this channel.