Study Lead Programmer | Remote (F/M)

Study Lead ProgrammerR Programming – Phase III Priority Clinical Studies What We OfferJoining our consulting team in Belgium means giving your career a step forward. Thanks to the privileged partnership we have with our well-established clients, leaders in their domain, we offer our consultants unique projects to develop their skills, and put their professional experience in the pharma industry on the fast track. As an expert on the client side, you can count on us to support you at each step of your project thanks to regular touch points with our Key Account Manager. We then also carefully choose with you what would be your next assignment that is matching your career goal whether it is in Consulting or in one of our Functional Services Platforms. We invest considerable time and resources in training our staff (technical and non-technical courses) to continuously support you in your personal and professional growth. On top of this, you will receive a complete remote-friendly engagement package tailored to your location within Europe, based on your background and experience. About the RoleWe are looking for an experienced Study Lead Programmer to take ownership of the statistical programming strategy for two Phase III priority clinical studies. You will act as the key point of technical oversight, ensuring programming deliverables are built to the highest quality standard and aligned with CDISC requirements throughout the study lifecycle. This is a fully remote assignment, open to candidates based in a European time zone, with an initial engagement of six months and extension expected based on project needs. Key ResponsibilitiesLead the statistical programming strategy across two Phase III priority clinical studiesProvide technical oversight and cross-verification of programming deliverables against CDISC standardsAct as the primary escalation point for programming-related risks, timelines and dependenciesDrive continuous improvement of programming tools, processes and ways of working Main ActivitiesOversee day-to-day programming activities across the two assigned studies, applying strong R programming skillsPerform cross-verification and quality oversight of deliverables produced by other programmersPropose and implement out-of-the-box ideas to accelerate delivery timelines and improve existing tools and processesSupport submission-related programming activities and ensure deliverables are ready for regulatory reviewMaintain proactive, transparent communication with study teams to meet stringent timelines Mandatory QualificationsPrevious experience as a Study Lead Programmer on clinical trialsProven experience and strong knowledge in either Oncology or Respiratory therapeutic areasStrong technical proficiency in R programming (upskilling support available where relevant)Solid working knowledge of CDISC standards (SDTM/ADaM) enabling cross-verification and oversight of programmersExperience with regulatory submissions is a strong assetFluent English required, French is an asset Our BenefitsJoining Astek means choosing an experience accelerator, where every assignment is an opportunity to progress; access to a multitude of technically exciting projects for our clients as well as internally; individualized, local support for a tailored career path; continuous learning, thanks to our internal training academy; and a friendly and inclusive work environment, supported by #TopEmployer2026 certified HR practices. Let's move forward.Alsinova - An Astek Company