Seal Beach, California3 days ago
Identify, qualify, manage, and maintain relations with clinical trial sites, including collaborating with Principal Investigators and field team to support robust and compliant study performance, drive site selection, patient recruitment programs to deliver enrollment targets. Oversee and approve clinical project deliverables such as scope definition documents, investigational product labeling, Pharmacy Manuals, informed consent forms, site activations, monitoring plan, CRFs, DMP, edit checks, safety plan, IDMC charter, close-out plans, and CSRs.