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At Allucent™, we are dedicated to helping small-medium biopharmaceutical companies efficiently navigate the complex world of clinical trials to bring life-changing therapies to patients in need across the globe. We're looking for a Senior Clinical Programmer I who thrives on solving complex challenges and transforming clinical data into high-quality, reliable insights that drive drug development. In this role, you'll play a key part in building and maintaining clinical databases, leading programming activities across global studies, and collaborating with cross-functional teams to deliver data that accelerates better outcomes for patients. Beyond study execution, you'll have the opportunity to influence departmental processes, mentor colleagues, and help shape the future of clinical programming within a collaborative and innovation-driven environment. About the Role As a Senior Clinical Programmer I , you will lead clinical programming activities that support the successful delivery of global clinical studies, ensuring high-quality data capture, database development, and regulatory compliance throughout the study lifecycle. You'll collaborate cross-functionally to design, build, validate, and maintain clinical databases, develop programming solutions and data visualizations, and champion CDISC standards and programming best practices. In addition to managing project timelines, budgets, and deliverables, you'll drive process improvements, contribute to business development activities, and provide technical leadership and mentorship to junior team members. Your main responsibilities will include but not limited to: Lead clinical programming activities across assigned studies, ensuring project timelines, budgets, deliverables, and resource needs are effectively managed while proactively identifying and escalating risks or change orders. Design, build, validate, and maintain clinical databases, electronic edit checks, data listings, and data visualization tools to support high-quality data collection, review, and regulatory compliance. Collaborate cross-functionally with Data Management, Project Management, Biostatistics, and study teams to develop study documentation, clarify technical specifications, and deliver programming solutions that meet project objectives. Champion industry standards and quality, applying CDISC conventions (CDASH, SDTM, TAUGs), validation principles, and programming best practices to ensure consistent, compliant, and inspection-ready deliverables. Drive innovation and continuous improvement by leading process enhancements, developing global programming standards and libraries, implementing data analytics and visualization tools, and supporting departmental initiatives. Requirements About You If you are a collaborative and detail-oriented clinical programming professional who enjoys solving complex technical challenges and takes pride in delivering high-quality, compliant data solutions that support global clinical trials. This role will give you the opportunity to combine strong expertise in clinical database programming, CDISC standards, and cross-functional collaboration with a passion for continuous improvement, mentoring others, and driving innovation in clinical data management. To be successful we are looking for the following traits and behaviors: Life science, healthcare, Computer Science and/or related field degree  Minimum 5 years of experience in drug development and/or clinical research  Good understanding and hands-on experiences of CDISC standards (i.e. CDASH, TAUGs and SDTM models)  Expert with electronic data capture (EDC) software systems and other tools for managing clinical studies  Expert in technical data management practices (developing programs, validation plans, testing, and documentation)    About Allucent Our mission is to help bring new therapies to light. When you work at Allucent, that means rolling up yo