Job summary
This role involves supporting the development of diagnostic imaging agents through scientific contributions to nonclinical projects, team support, and process improvement. The position focuses on non-laboratory-based activities within a broad portfolio of imaging products at various development stages, aiding regulatory and lifecycle processes.
Location and work setup
- Location
- Oslo
- Work setup
- Hybrid
Responsibilities
Contribute scientific expertise in biology, pharmacology, toxicology or related life-science disciplines to nonclinical development programs. Support effective team operations across multiple projects. Identify and implement process simplifications and improvements. Assist in the design, planning, conduct, and interpretation of in vitro and in vivo nonclinical studies. Take responsibility for defined scientific activities with an appropriate degree of independence. Support preparation and review of scientific and regulatory documentation including reports and submissions. Provide cross-program scientific support and act as subject matter expert for projects, including addressing inquiries from external parties such as health authorities.
Qualifications
MSc or PhD in Biology, Pharmacology, Toxicology, Life Sciences, or equivalent experience. Experience or knowledge in cardiology, neurology, or oncology related to therapeutic or diagnostic drug development. Familiarity with imaging modalities (PET, SPECT, CT, MR, ultrasound) is desirable but not essential. Prior experience with regulatory submissions, GLP safety studies, and risk assessments is preferred but not required. Strong initiative, independent and systematic working style. Excellent English communication skills and collaboration abilities.