Make your mark for patients We are looking for a Senior Principal Programmer (Statistical Computing ... You understand CDISC standards, including SDTM and ADaM, and have worked with Tables, Figures, and ...
Make your mark for patients We are looking for a Senior Principal Programmer (Statistical Computing ... You understand CDISC standards, including SDTM and ADaM, and have worked with Tables, Figures, and ...
Make your mark for patients We are looking for a Senior Principal Programmer (Statistical Computing ... You understand CDISC standards, including SDTM and ADaM, and have worked with Tables, Figures, and ...
Make your mark for patients We are looking for a Senior Principal Programmer (Statistical Computing ... You understand CDISC standards, including SDTM and ADaM, and have worked with Tables, Figures, and ...
... senior management. * Participate and/or lead in strategic initiatives, special projects, and ... SDTM), or analysis (ADaM) models. * At least 8 years of clinical database developer experience in ...
... senior management. * Participate and/or lead in strategic initiatives, special projects, and ... SDTM), or analysis (ADaM) models. * At least 8 years of clinical database developer experience in ...
... senior management. * Participate and/or lead in strategic initiatives, special projects, and ... SDTM), or analysis (ADaM) models. * At least 8 years of clinical database developer experience in ...
... senior management. * Participate and/or lead in strategic initiatives, special projects, and ... SDTM), or analysis (ADaM) models. * At least 8 years of clinical database developer experience in ...
Senior Sdtm Programmer information
What is the difference between Senior Sdtm Programmer vs Clinical Data Coordinator?
| Aspect | Senior Sdtm Programmer | Clinical Data Coordinator |
|---|---|---|
| Credentials | Typically requires a degree in life sciences or related field, with experience in SDTM programming | Usually holds a degree in health sciences, nursing, or related field, with data management training |
| Work Environment | Works primarily in clinical trial data programming, using SAS or similar tools | Manages data entry, cleaning, and validation in clinical trial settings |
| Industry Usage | Commonly employed in pharmaceutical and biotech companies for SDTM data standardization | Found in clinical research organizations, hospitals, and pharmaceutical companies |
The main difference is that Senior Sdtm Programmers focus on programming and data standardization using SDTM standards, while Clinical Data Coordinators handle data collection, entry, and quality control. Both roles are essential in clinical trials but differ in technical scope and responsibilities.
What are the typical collaboration points between a Senior SDTM Programmer and clinical data management teams?
As a Senior SDTM Programmer, you frequently collaborate with clinical data management teams to ensure data collected from clinical trials is accurately mapped and transformed into SDTM-compliant datasets. This often involves clarifying data specifications, resolving data discrepancies, and aligning on timelines for data delivery. Close communication helps maintain data integrity and compliance with regulatory standards, making teamwork and proactive problem-solving crucial aspects of the role.
What are Senior SDTM Programmers?
Senior SDTM Programmers are experienced professionals in clinical data management who specialize in mapping and converting clinical trial data into the Study Data Tabulation Model (SDTM) format according to regulatory requirements. They ensure that data collected during clinical trials is structured, accurate, and compliant with standards set by organizations like the FDA and CDISC. Senior SDTM Programmers often lead programming activities, perform quality control checks, and collaborate with statisticians, data managers, and regulatory teams to prepare submission-ready datasets. Their expertise is vital for successful clinical trial submissions and regulatory approvals.
What are the key skills and qualifications needed to thrive as a Senior SDTM Programmer, and why are they important?
To excel as a Senior SDTM Programmer, you need deep expertise in clinical data standards (especially CDISC SDTM), advanced SAS programming skills, and a relevant degree in life sciences, statistics, or computer science. Familiarity with clinical trial data management systems, regulatory submission requirements, and tools like Pinnacle 21 are also crucial. Strong attention to detail, problem-solving abilities, and effective communication skills help ensure data accuracy and smooth collaboration with cross-functional teams. These competencies are essential to deliver high-quality, regulatory-compliant datasets that support successful clinical trial submissions.
What are popular job titles related to Senior Sdtm Programmer jobs in Georgia? For Senior Sdtm Programmer jobs in Georgia, the most frequently searched job titles are:
What job categories do people searching Senior Sdtm Programmer jobs in Georgia look for? The top searched job categories for Senior Sdtm Programmer jobs in Georgia are:
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.
About UCB
Sourced by ZipRecruiter
Industry
Finance and insurance
Company size
1,001 - 5,000 Employees
Headquarters location
Toledo, OH, US
Year founded
1959