Join Clario’s industry-leading Digital Physiology team as a Principal Statistical Programmer, where your expertise will drive innovation in clinical research. This is a unique opportunity to lead advanced statistical programming for cardiac safety trials, shaping the future of digital health through cutting-edge data science and global collaboration.
What we offer
Competitive compensation + shift allowances
Attractive benefits (security, flexibility, support and well-being)
Engaging employee programs
Technology for hybrid working and great onsite facilities
What you'll be doing
Statistical Programming & Data Standards
Lead and coordinate all statistical programming activities for cardiac safety trials.
Develop, test, and maintain SAS code to generate CDISC-compliant datasets (SDTM, ADaM).
Produce and maintain submission-ready datasets and electronic submission packages (e.g., define.xml, reviewer’s guide) in accordance with FDA guidelines.
Team Leadership & Mentorship
Manage direct reports in a line or matrix capacity, including work allocation, resource planning, and professional development.
Conduct onboarding and training on statistical programming practices and SOPs.
Mentor junior staff and provide guidance on programming methodologies and quality standards.
Process Improvement & Strategic Initiatives
Identify and implement process improvements to enhance operational efficiency.
Develop and maintain SOPs, SWIs, templates, and playbooks for programming deliverables.
Drive initiatives for future analyses, data quality, and standardization.
Cross-functional Collaboration & Project Management
Collaborate with cross-functional teams to define scope and timelines for statistical deliverables.
Manage client commitments and ensure timely delivery of assigned projects.
Maintain accurate tracking of deliverable statuses and dates.
What we're looking for
Ph.D. with 5+ years of relevant industry experience, M.S. with 7+ years of relevant industry experience or B.S. with 10+ years of relevant industry experience
A degree in medical, health, public, or general science—or an equivalent combination of education and experience sufficient to perform job duties
Strong experience in clinical trials, preferably within a CRO or pharmaceutical research organization
Proficiency in SAS programming, including creation, testing, and maintenance of CDISC-compliant datasets (SDTM, ADaM)
Experience with electronic submission packages and regulatory interactions (e.g., FDA)
Familiarity with clinical protocols and Statistical Analysis Plans
Experience with TFL generation is a plus
Solid understanding of the pharmaceutical drug development process
At Clario, our purpose is to transform lives by unlocking better evidence. It’s a cause that unites and inspires us. It’s why we come to work—and how we empower our people to make a positive impact every day. Whether you're advancing clinical science, building innovative technology, or supporting our global teams, your work helps bring life-changing therapies to patients faster.
