Genmab is looking to solve the problem of developing innovative antibody products and groundbreaking medicines that change lives and the future of cancer treatment and serious diseases.
Requirements
- Basic knowledge of programming concepts; exposure to SAS, R, or other statistical software is preferred.
- Interest in clinical data standards (e.g., CDISC SDTM, ADaM) and regulatory guidelines.
- Develop and maintain up-to-date knowledge of relevant ICH guidelines, regulatory guidelines, statistical concepts, CDISC fundamentals and therapeutic-area basics.
- Knowledge of data manipulation, data visualization, and reporting
- Familiarity with version-control discipline and good programming practices
- Understanding of company standard coding
Responsibilities
- Execute programming activities (including but not limited to development of SDTM, ADaM, TLF) under close supervision, focusing on assigned tasks or components of deliverables as directed by Trial Programming Lead.
- Conduct QC or sponsor oversight under close supervision.
- Develop proficiency in the use of company standard coding.
- Build technical skillset in data manipulation, data visualization, and reporting.
- Participate in internal programming meetings and required training sessions.
- Maintain up-to-date knowledge of relevant study level documents
- Contribute to documentation in support of inspection readiness
Other
- 0 years relevant experience; entry-level role
- Bachelor’s or Master’s degree in statistics, biostatistics, computer science, or a related field.
- Strong attention to detail and organizational skills.
- Ability to work effectively as part of a collaborative team in a fast-paced environment.
- You are genuinely passionate about our purpose
