Teams at Allucent

Coordinates clinical study site start-up activities from initial preparation through Site Initiation Visit. Responsibilities include tracking milestones in CTMS, filing eTMF records, preparing IEC/IRB submissions, adapting informed consent forms, collecting and reviewing essential documents, resolving discrepancies, and handing sites over to CRAs. The role may also support feasibility, site identification, and clinical agreement or budget negotiations.

Lead population PK/PD modeling and simulation projects, design and interpret clinical pharmacology studies, mentor pharmacometricians, provide strategic regulatory guidance and author regulatory documents, manage client relationships, and support business development to advance drug development programs.