> Markdown version of [/jobs/ext/3587063-programming-manager-clinical-programming](https://www.wearedevelopers.com/jobs/ext/3587063-programming-manager-clinical-programming). Every page supports `.md` or `Accept: text/markdown`. Links point to the HTML versions so they work for humans too. Agent guide: [/agents.md](https://www.wearedevelopers.com/agents.md). --- # Programming Manager, Clinical Programming - **Company:** Genmab Inc - **Location:** Plainsboro Township, NJ, United States - **Experience:** Experienced - **Salary:** $117,840.0 - **Contract:** Permanent contract - **Skills:** Computer Programming, Databases, Data Structures, SAS (Software), Software Requirements Analysis, Information Technology - **Published:** October 5, 2026 - **Apply:** https://find.jobs/jobs-near-me/apply/ats-redirect/?id=3005342033-2 ## About the Role * Bachelor's degree in Statistics, Computer Science, Life Sciences. Master's degree in Statistics, Computer Science, Life Sciences preferred * Has experience working in a global context * Proficient in both written and spoken English * At least 3-5 years of experience within the pharmaceutical industry * Has experience with the SAS software package, * SAS programming * Analytical and problem-solving skills * Expert knowledge of the CDISC SDTM data model: the corresponding structures and organizations of the data. * Contextual understanding of the data * Writes efficient, easily maintained and well documented computer programs * Is systematic and organized in writing and archiving computer programs * Proactive and Accountable and Goal oriented * Innovative * Good team player * Good at sharing knowledge * Works independently, take responsibility and show initiative * Good communication skills * Good planning and coordinating skills * Ability to flexibly work on multiple tasks without compromise of the quality of the work ## Description Work arrangement: This role offers flexibility to work away from the office for 20%-40% of a typical schedule. Employees may use this work schedule in increments of single days or multiple consecutive days, provided it does not exceed 40% within a 60-day period, and is approved by the hiring manager., * Implements and assists on developing company Study Data Tabulation Model (SDTM) standards that support the scientific need of a study/program while ensuring quality, consistency and compliance to CDISC standards and other industry standards that supports the exchange of data, reporting, and analysis * Ensures alignment of SDTM standards with data collection standards and relevant company tools/system requirements by reviewing study eCRFs, supporting creation of external data collection standards, and providing SDTM mapping guidance * Ensures study or portfolio-level SDTM datasets are in compliance with CDISC and regulatory submission requirements, reviews study submission data packages to ensure quality and integrity * Creates quality control processes, metrics and other measures to ensure compliance with standards * Ensures work carried out in accordance with applicable SOP's and working practices, as well as global agency regulations/guidance's * Supports developing and reviewing standard processes and templates. * Working with Digital Solutions and IT, support the implementation of future strategies and technology-enabled processes and tools for clinical trials standards, change control management and the exchange of standards information to internal downstream consumers and externally consumers * Supports development of GenSense Dashboards by providing guidance on data structure, organization and contents of the Genmab SDTM-databases to the Dashboard developers and programmers * Produce other in-house checks of data consistencies * Contributes to knowledge sharing, skill building and good collaboration with stakeholders and colleagues * Contributes to ongoing improvements in cross-functional and global collaboration and sharing of better practices and knowledge * Maintains up-to-date knowledge on relevant regulatory guidelines/requirements * Maintains a good working relationship with stakeholders and colleagues * Participates and represent clinical programming in teams and meetings, As Programming Manager, Clinical Programming, it is expected that the employee: * Acts as a role model * Leads programming study team in an effective and professional manner * Proactively engages in department activities * Arranges lessons learned to share learnings * Leads various initiatives within the department Proactively contributes to support a global organization * Acts as mentor for new employees or consultants