Posted on 11/05/2024

Mid-Level Clinical SAS Programmer

Experience: 3+ Years, Salary: Not disclosed, Job Code (JPC - 1016), Location: Bedford, Nashua, USA,

Clinical SAS

About the Role:

We’re looking for a skilled Clinical SAS Programmer with at least 3 years of experience to join our team and support our clinical research efforts. In this role, you’ll work directly with clinical data and statistical teams to transform complex data into meaningful insights, helping to drive critical decisions in our research. This is a great opportunity if you enjoy working with data and want to contribute to impactful studies in a collaborative environment.

As a Mid-Level Clinical SAS Programmer, you’ll be responsible for developing and validating datasets, tables, listings, and figures (TLFs) that support clinical study reports and regulatory submissions. You’ll play an essential role in maintaining data accuracy, quality, and compliance with industry standards, working closely with a team of experienced professionals to make sure our data tells a clear, accurate story.

Project Role

Mid-Level Clinical SAS Programmer

What You’ll Be Doing:

Your work will help ensure that our clinical data meets the highest standards and supports effective decision-making:
Create and Validate Datasets: Develop and validate analysis datasets (e.g., SDTM, ADaM) using SAS programming to ensure they align with clinical study requirements.
Generate TLFs: Produce tables, listings, and figures that accurately represent study findings, working with statisticians to interpret and present results clearly.
Quality Control: Perform quality checks on datasets and TLFs to ensure accuracy, consistency, and compliance with CDISC standards and regulatory guidelines.
Collaborate with Study Teams: Work closely with statisticians, data managers, and other team members to understand study requirements, troubleshoot issues, and support project needs.
Support Regulatory Submissions: Assist in preparing data outputs for FDA, EMA, and other regulatory submissions, ensuring that all outputs meet compliance standards.
Document and Report Programming Processes: Maintain clear documentation of programming procedures and datasets for future reference and audit readiness.

What We’re Looking For:

We’re looking for a detail-oriented, analytical professional who loves working with data and thrives in a team environment:

3+ Years of SAS Programming Experience: Previous experience in clinical SAS programming, ideally within a clinical research, CRO, or pharmaceutical setting.
Technical Skills: Proficiency in SAS programming, with a good understanding of CDISC standards (SDTM, ADaM) and the ability to work with complex clinical datasets.
Problem-Solving Mindset: You have a knack for troubleshooting data issues and finding solutions that meet project requirements.
Attention to Detail: Strong commitment to data quality and accuracy, with a focus on compliance with regulatory standards.
Communication Skills: Ability to collaborate effectively with team members and communicate technical details in a clear, accessible way.

Skills Required:

Strong SAS programming skills, experience with CDISC standards (SDTM, ADaM), knowledge of clinical trial processes, problem-solving skills.

Why You’ll Love This Role:

This role offers a unique chance to work on meaningful clinical research projects in a supportive, collaborative team. You’ll have the opportunity to develop your programming skills, work with cutting-edge tools, and contribute to studies that make a real difference. If you’re passionate about data, enjoy solving complex problems, and want to grow your career in clinical programming, we’d love to have you on board!