Bone substitute materials permissive for trans-scaffold migration and in-scaffold survival of human bone-derived cells are mandatory to develop cell-engineered permanent implants to repair bone defects. In this study, we evaluated the influence on human bone-derived cells of the material composition and microstructure of foam scaffolds made from calcium aluminate using a direct foaming method allowing wide-range tailoring of the microstructure for pore size and pore openings. Human fetal osteoblasts attached to the scaffolds, migrated across the entire materials depending on the scaffold pore size, colonized and survived in the porous material for at least 6 weeks. The long-term biocompatibility of the scaffold material for human cells was evidenced by in scaffold determination of cell metabolic activity using a modified MTT assay, a repeated WST-1 assay and scanning electron microscopy. Finally, we demonstrated that the fetal cells can be covalently bound to the scaffolds using biocompatible click chemistry, thus enhancing the rapid adhesion of the cells to the scaffolds. Thus, the different microstructures of the foams influenced the migratory potential of the cells, but not cell viability, and the scaffolds were permissive for covalent biocompatible chemical binding of the cells to the materials, allowing either localized or widespread cellularization of the scaffolds for cell-engineered implants.