Location: Remote/On-Site
Contract-Based Position
At Beaufort CRO, we’re committed to improving lives through the rapid development and commercialization of groundbreaking life science products. We specialize in in-vitro diagnostics (IVD), medical devices, and pharmaceuticals, supporting our clients in bringing innovative products to market faster. We’re seeking a Statistical Programmer for a contract-based position to support our life science client projects, including clinical trial studies.
If you’re an experienced SAS programmer with a deep understanding of clinical trial data, particularly in IVD, and you're looking to make an impact, this is the opportunity for you!
Your Role and Responsibilities:
As a Statistical Programmer at Beaufort, you’ll be the key player in supporting the development of high-quality statistical analysis for clinical trials. Your tasks will include:
- Review & Planning: Engage in pre-project activities, such as reviewing Protocols, Case Report Forms (CRFs), Statistical Analysis Plans, and Programming Plans.
- Data Creation & Analysis: Once the plans are approved, you will create analysis datasets and perform the necessary statistical analyses to meet project specifications.
- Validation & Modification: Ensure the statistical analyses align with the plan and validate accordingly. Adapt to client changes and modifications as needed.
- Documentation & Reporting: Provide clear and comprehensive documentation logs. Finalize the analysis and prepare reports, including tables, listings, and figures for the Clinical Study Report (CSR).
- Archiving: Organize and archive all documentation to ensure regulatory compliance and quality standards are met.
- Other Project Tasks: Support other project-related tasks as specified in the Statement of Work.
What We’re Looking For:
- Education: Minimum Bachelor’s Degree in a relevant field.
- Experience: At least 5 years of experience as a Statistical Programmer, with a strong background in SAS programming and clinical trial data analysis. Experience in in-vitro diagnostic trials is highly desirable.
- Technical Skills:
- Proficiency in SAS programming and a deep understanding of industry standards.
- Familiarity with clinical trial data, especially for IVD.
- Non-Technical Skills:
- Effective communication skills (both verbal and written) to clearly document findings and collaborate with cross-functional teams.
- A collaborative work style and the ability to work in a team-focused environment.
Why Beaufort CRO?
- Impact: You’ll be part of a team that’s making a difference by helping life science companies improve and save lives.
- Culture: We’re not just about what we do, but how we do it. Join a company that fosters a culture of excellence, passion, and commitment.
- Industry-Leading Expertise: Work with experts specializing in IVD, clinical project management, and regulatory solutions.
- Collaboration: Work in an environment where accountability and teamwork are central to our success, helping clients achieve successful market authorization.
Join Us
At Beaufort, you’ll work alongside industry leaders, contribute to innovative projects, and help shape the future of life-saving technologies. If you’re ready to take your career to the next level and contribute to meaningful change, we’d love to hear from you.
Beaufort CRO is an equal opportunity employer, and we value diversity in our team. We encourage individuals from all backgrounds to apply.
