Senior Clinical Programmer

Allucent

Senior Clinical Programmer I leading clinical programming activities for global studies at Allucent. Collaborating across teams to ensure high-quality data and regulatory compliance in clinical trials.

Posted 6/26/2026full-timeRemote • 🇺🇸 United StatesSeniorWebsite

ATS Keywords

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Hard Skills

clinical programmingdata managementprogramming solutionsdata analyticsdata visualizationvalidation principlesprogramming best practiceselectronic edit checksclinical databasestechnical data management

Soft Skills

leadershipcollaborationproject managementrisk managementinnovationcontinuous improvementcommunicationproblem-solvingresource managementquality assurance

Tools & Technologies

EDC software systemsdata visualization toolsclinical databasesdata listingsCDISC standardsCDASHSDTMTAUGsvalidation planstesting documentation

Industry Keywords

clinical researchdrug developmentregulatory compliancelife scienceshealthcareglobal programming standardsprocess enhancementsinspection-ready deliverablesstudy documentationcross-functional collaboration

About the role

Key responsibilities & impact

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

What you’ll need

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)

Benefits

Comp & perks

Comprehensive benefits package per location
Competitive salaries per location
Departmental Study/Training Budget for furthering professional development
Flexible Working hours (within reason)
Opportunity for remote/hybrid* working depending on location
Leadership and mentoring opportunities
Participation in our enriching Buddy Program as a new or existing employee
Internal growth opportunities and career progression
Financially rewarding internal employee referral program
Access to online soft-skills and technical training via internal platforms
Eligibility for our Spot Bonus Award Program in recognition of going above and beyond on projects
Eligibility for our Loyalty Award Program in recognition of loyalty and commitment of longstanding employees