Senior Programming Associate

1 week ago

Copenhagen, Copenhagen, Denmark Genmab Full time

The ideal candidate will be responsible for ensuring the integrity and consistency of data across various clinical trials, adhering to standards such as CDISC, SDTM, and ADaM. This role will involve reviewing CRFs, supporting the establishment and maintenance of database standards, and performing consistency checks on databases delivered by vendors.

Main Responsibilities:

  • Reviews CRFs for adequacy and consistency
  • Supports the establishment and maintenance of Genmab SDTM and ADaM database standards
  • Performs database standards consistency checks on databases delivered by the preferred DM & Statistics vendor to Genmab
  • Produces other in-house checks of data consistencies
  • Supports specification and pooling of data across clinical trials within the same project
  • Supports in-house production of analysis datasets, tables, figures, and listings by writing the corresponding programs and ensuring QC before formal release
  • Aids in sponsor oversight of programming activities on the DM & Statistics vendor
  • Performs QC on SAS-code written by other Genmab colleagues
  • Supports submissions by ensuring that the programming-related part of the file is consistent with current electronic submission standards and guidelines
  • Provides feedback on application development within the department when requested
  • Supports resource planning and outsourcing of programming activities
  • Supports developing and reviewing standard processes and templates
  • Contributes to knowledge sharing, skill building, and good collaboration with stakeholders and colleagues

Requirements:

  • Has experience with the SAS software package and other programming languages (such as R and Python)
  • Minimum Bachelor of Science degree or equivalent qualifications
  • Proficient in both written and spoken English
  • At least 2 years of experience within the pharmaceutical industry as a Programmer (for Senior Programming Associate level)

About the Role:

This role will be based in Genmab's office in Princeton, NJ USA; Copenhagen, Denmark; or Utrecht, the Netherlands and is hybrid. Applicants who are not within local commuting distance could be considered for remote-based work, with strong preference for those based in Eastern or Central Time Zones (US) or European time zones in Copenhagen, Denmark and Utrecht, the Netherlands.

Competences and Skills:

  • SAS programming
  • Analytical and problem-solving skills
  • Knowledge of the CDISC, SDTM, and ADaM data models, including the corresponding structures, and organizations of the data
  • Contextual understanding of the data
  • Ability to write efficient, easily maintained, and well-documented computer programs
  • Systematic and organized in writing and archiving computer programs
  • Thorough
  • Proactive, Accountable, and Goal-Oriented
  • Innovative
  • Good team player
  • Good at sharing knowledge
  • Works independently, takes responsibility, and shows initiative
  • Good communication skills
  • Good planning and coordinating skills
  • Ability to flexibly work on multiple tasks without compromising the quality of the work

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