The Clinical Trial Pharmacist is a member of the Site Principal Investigator’s site team. They are responsible for the management of investigational products including medicines and biologicals but may also manage gene therapy and radiopharmaceuticals.
They should participate in the feasibility of the trial at the site, site selection visit and site initiation visit. Once the trial is ready to commence, responsibilities include supply ordering, handling, storage, dispensing, accountability and destruction in accordance with the current approved trial protocol.