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 offerCompetitive compensation + shift allowancesAttractive benefits (security, flexibility, support and well-being)Engaging employee programsTechnology for hybrid working and great onsite facilitiesWhat you'll be doingStatistical Programming & Data StandardsLead 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.Create and implement data standards and macros to support cardiac safety deliverables.Research and apply new programming techniques to enhance data processing and analysis.Generate and interpret compliance checks on CDISC-formatted datasets.Support statistical analyses and regulatory requirements through client-facing discussions.Team Leadership & MentorshipManage 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.Lead team strategy meetings and contribute to departmental planning.Process Improvement & Strategic InitiativesIdentify 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.Participate in hiring and contribute to strategic planning for the statistical programming function.Cross-functional Collaboration & Project ManagementCollaborate 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.Provide consultation during sponsor and regulatory teleconferences (FDA, EMEA, PMDA).What we're looking forPh.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 experienceA degree in medical, health, public, or general science—or an equivalent combination of education and experience sufficient to perform job dutiesStrong experience in clinical trials, preferably within a CRO or pharmaceutical research organizationProficiency 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 PlansExperience with TFL generation is a plusSolid understanding of the pharmaceutical drug development processProficient in Windows and Microsoft Office productsDemonstrated leadership experience and/or trainingExcellent verbal and written communication skillsStrong organizational and analytical abilitiesAbility to work both independently and in a team setting, with flexibility to adapt to changing prioritiesAt Clario, we put people first, always. We are united and driven by patients, committed to making a difference, and we are always looking for the best talent to help us transform lives. We value the contribution each of our people brings. It’s only through our people that we can continue to innovate technology that will shape the future of clinical trials.
