Posted on 11/05/2024

Senior Clinical SAS Programmer

Experience: 7+ Years, Salary: Not disclosed, Job Code (JPC - 1017), Location: Bedford, Nashua, USA
Clinical SAS

About the Role:

Are you ready to take on a senior-level role where your clinical programming expertise can truly make a difference? We’re looking for a Senior Clinical SAS Programmer with 7+ years of experience to join our team. In this role, you’ll have the opportunity to lead impactful projects, work with complex data, and mentor others, all while helping us advance healthcare through data-driven insights. If you enjoy a mix of hands-on programming, strategic project oversight, and cross-team collaboration, this could be the perfect fit.

As our Senior Clinical SAS Programmer, you’ll be at the forefront of developing, validating, and documenting SAS programs for clinical trials. Your work will involve creating datasets, tables, listings, and figures (TLFs) that are essential for clinical study reports and regulatory submissions. You’ll be a crucial part of a dedicated team, working closely with statisticians, data managers, and other professionals to ensure our data is accurate, compliant, and insightful.
Project Role

Senior Clinical SAS Programmer

What You’ll Be Doing:

Your responsibilities will span from hands-on programming to leading projects and supporting a talented team:

  • Design and Validate Complex Datasets: Lead the development of analysis datasets (e.g., SDTM, ADaM) using SAS programming to meet study requirements and maintain CDISC compliance.
  • Generate and Review Clinical Reports: Create and validate tables, listings, and figures that effectively present trial findings, helping the team deliver clear, reliable data reports.
  • Ensure Data Quality and Troubleshoot Issues: Perform quality checks on datasets and outputs, proactively identifying and solving issues to maintain the integrity of our data.
  • Prepare for Regulatory Submissions: Work on data outputs for regulatory submissions, including FDA and EMA, ensuring all outputs are compliant with regulatory standards and guidelines.
  • Mentor and Guide Junior Programmers: Share your expertise through mentorship and code reviews, helping junior team members learn best practices and supporting their professional growth.
  • Collaborate Across Teams: Partner with statisticians, data managers, and other team members to ensure data aligns with project needs, timelines, and industry standards.

What We’re Looking For:

We’re seeking a skilled, collaborative professional who can balance technical expertise with strong team leadership:

  • 7+ Years of Clinical SAS Programming Experience: Extensive experience in clinical SAS programming, ideally within a clinical research, pharmaceutical, or CRO setting.
  • Advanced Technical Skills: Proficiency in SAS programming, with deep knowledge of CDISC standards (SDTM, ADaM) and an understanding of FDA and EMA submission processes.
  • Leadership and Mentorship Skills: Experience guiding junior team members, managing project timelines, and fostering a collaborative work environment.
  • Strong Attention to Detail: A commitment to data accuracy and regulatory compliance, with a keen eye for identifying and resolving inconsistencies.
  • Excellent Communication and Collaboration Skills: You can translate complex programming concepts for team members and enjoy working alongside a diverse group of professionals.

Skills Required:

Advanced SAS skills, expertise in CDISC standards, experience with regulatory submissions, leadership, and project management abilities.

Why You’ll Love This Role:

This is a chance to step into a role where your experience and insights are valued. You’ll work on meaningful clinical studies that contribute to health advancements, using your skills to deliver data that informs critical decisions. You’ll also have the opportunity to mentor others, share your knowledge, and take a leadership role within a supportive, collaborative team. If you’re ready to bring your clinical programming expertise to a place where it can truly make an impact, we’d love to meet you. This role offers growth, challenge, and the satisfaction of knowing your work has real-world benefits.

At Fourhub, we are dedicated to providing equal employment opportunities.

Share your resume with us, and we’ll be in touch as soon as we find a role that’s a great fit for your skills and experience.