Fundamental understanding of the charge (ions and water) transport in polymeric membranes used at the forefront of the water-energy nexus challenge is yet uncertain and depends on the complex interplay between polymer structure and dynamics that facilitate transport. Herein, we investigated the dynamics-transport of proton and ion transport in a rather neutrally charged organic membrane (i.e., polyamide) using solid-state NMR spectroscopy. Specifically, the role of competing ions' effect in complex ionic mixtures at the membrane interface has been explored on a molecular level. Proton and sodium ion diffusion measurements are made using pulsed-field gradient NMR diffusometry. The energy barriers for proton and ion transport within the active layer of the reverse osmosis (RO) membrane are assessed using magic angle spinning (MAS) and static NMR spectral line shape analysis. We have investigated the dynamics-transport of water and sodium ions in complex ionic mixtures of polyamide polymeric media using solid-state NMR spectroscopy. Through monitoring ¹³C, ²³Na, and ¹H NMR nuclei, quantitative insights into the diffusion of water (¹H), sodium mobile ion (Na⁺), and polymer membrane dynamics (¹³C) are extrapolated. Furthermore, the spin-lattice (T₁) relaxation time of sodium and water ions is investigated to obtain quantitative insight into how sodium and water ions’ rotational movements occur in the absence and presence of other competing seawater cations such as potassium. Room temperature spectra and spin-lattice relaxation times indicated the presence of both mobile and rigidly held ionic species in the membrane at different levels of relative humidity. The concentration and temperature dependence of relaxation times and chemical shifts have been investigated. NMR relaxation measurements detect how the water rotation is modified by sodium and potassium cations in the membrane. Results show that at low relative humidity and in the presence of competing ions, there are sodium ion resonances for crystalline sodium ions and rigidly held sodium ions on the surface. With increasing relative humidity and decreasing competing ions, the resonance suggests solution-like dynamic rotational movements of sodium ions in polyamide. The results confirm the change in activation energy barrier for sodium and hydrogen ion permeation in polyamide upon the presence of potassium ions.