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Oscillatory synchrony is hypothesized to support the flow of information between brain regions, with different phase-locked configurations enabling activation of different effective interactions. Along these lines, past work has proposed multistable phase-locking as a means for hardwired brain networks to flexibly support multiple functional patterns, without having to reconfigure their anatomical connections. Given the potential link between interareal communication and phase-locked states, it is thus important to understand how those states might be controlled to achieve rapid alteration of functional connectivity in interareal circuits. Here, we study functional state control in small networks of coupled neural masses that display collective multistability under determinstic conditions, and that display more biologically-realistic irregular oscillations and transient phase-locking when conditions are stochastic. In particular, we investigate the global responses of these mesoscale circuits to external signals that target only a single subunit. Focusing mainly on the more realistic scenario wherein network dynamics are stochastic, we identify conditions under which local inputs (i) can trigger fast transitions to topologically distinct functional connectivity motifs that are temporarily stable ("state switching"), (ii) can smoothly adjust the spatial pattern of phase-relations for a particular set of lead-lag relationships ("state morphing"), and (iii) fail to regulate global phase-locking states. In total, our results add to a growing literature highlighting that the modulation of multistable, interareal coherence patterns could provide a basis for flexible brain network operation.