Senior Statistical Programmer
Location: Syneos Health, Global
About Syneos Health
Syneos Health is a global leader in biopharmaceutical solutions, focusing on accelerating customer success by translating clinical, medical affairs, and commercial insights into real-world outcomes. With a mission to bring customers and patients to the center of everything, Syneos Health aims to simplify the clinical development process. With over 29,000 employees across 110 countries, we’re committed to making a meaningful difference in the lives of patients.
"Work Here Matters Everywhere."
Why Syneos Health?
We are passionate about developing our people. Our Total Self culture promotes career development, mentorship, and diversity, creating a workplace where everyone can thrive. We support your growth through technical and therapeutic training, a peer recognition program, and a rewards structure.
By fostering diverse perspectives, we create an environment where people feel they belong.
Key Responsibilities
Programming & Data Management:
Use SAS or other software to develop custom programming code for generating summary tables, data listings, graphs, and derived datasets in accordance with the statistical analysis plan.
Ensure programming outputs meet quality standards and project requirements. Perform validation programming and resolve discrepancies with team members.
Maintain organized and up-to-date project documentation for quality control and inspection readiness.
Collaboration & Leadership:
Act as Lead Statistical Programmer, overseeing and guiding the programming activities of other programmers.
Manage and prioritize programming tasks across multiple projects, ensuring deliverables are met on time.
Participate in meetings with sponsors, contributing insights and ensuring accurate communication of project status.
Mentor junior programmers through training courses, presentations, and performance feedback.
Project Delivery & Risk Management:
Manage scheduling and deadlines, adapting to changes in project timelines or priorities.
Negotiate and establish accurate time estimates for programming activities, ensuring projects stay on track.
Review project documentation, such as the Statistical Analysis Plan and programming specifications, providing feedback that minimizes inefficiencies.
Compliance & Standards:
Follow applicable SOPs and regulatory guidelines (e.g., ICH) to ensure compliance in all programming tasks.
Assist in ensuring project deliverables meet CDISC Standards (SDTM, ADaM, DEFINE.XML) and contribute to regulatory submissions.
Maintain knowledge of industry standards and regulatory changes, incorporating this knowledge into project work.
Qualifications
Education & Experience:
Undergraduate degree in a scientific or statistical discipline, or an equivalent combination of education and programming experience.
Extensive experience in SAS programming within a clinical trial environment.
Excellent written and verbal communication skills with proficiency in English.
Skills & Competencies:
Strong organizational skills, with the ability to manage multiple projects simultaneously.
Experience mentoring and guiding junior programming staff.
In-depth knowledge of clinical trial processes, regulatory standards, and industry guidelines.
Why Work with Us?
Career Growth: Opportunities for advancement and professional development in a dynamic and growing company.
Inclusive Culture: Join a diverse and inclusive team that values every individual’s contributions.
Meaningful Work: Play a key role in the development of therapies that impact patient lives around the world.
Additional Information:
Syneos Health is committed to equal opportunity and diversity. If your experience doesn’t match the job description perfectly, we encourage you to apply. Your transferrable skills may be exactly what we need.
Minimal travel may be required.
Apply Now to be part of a forward-thinking team dedicated to delivering therapies that matter.
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