You don't necessarily have to work on a grant specific project or a healthcare team this is more academic institutional research. In clinical research, a pharmacist would be able to work for pharma companies and CROs. You could work as a project manager if you aren't looking to help dispense medications for specific study sites. Project managers help negotiate contracts with vendors specific to the study, prepare timelines for keeping the developmental process on track, and work with study budgets. You could also head up a pharmacovigilance department that handles all adverse events that come in for specific studies, assessing seriousness and notifying sponsor and the FDA of these events. If you worked on the regulatory side, your role would be to take care of all FDA submissions from the IND to the NDA. There are 3 phases to the drug development process that takes you up through approval of a drug. However, you can have phase 4 studies, which are post-marketing studies that occur after the drug has been approved.