Clinical Science Program Specialist - Tucson

Clinical Science Program Specialist – CDx Pharma Services (requisition). The pay rate is /hr with a maximum client bill rate of /hr. Opportunity Manages multiple clinical testing and lab services projects from initiation through contract completion under supervision of Program Manager. Acts as primary point of contact to Pharma customers. Develops project plans, establishes and coordinates timelines for assigned projects and functions. Manages execution of cross‑functional plans and tracks progress of activities. Identifies gaps, potential bottlenecks or delays and challenges assumptions. Oversees and guides day‑to‑day activities of sample process flow and accurate reporting of results. Implements best practices within the clinical sciences team; fosters continuous improvement by ensuring knowledge and experience exchange. Guides and manages cross‑functional interactions to complete assigned projects within the deadline. Interfaces with resources outside the company (Contract Research Organizations (CROs), site investigators, client counterparts, etc.) and serves as single point of contact with Pharma and Roche clients. Manages meeting activities such as setting agendas, organizing meeting time and editing meeting minutes. Tracks, maintains and communicates project reports and clinical study data to Pharma and Roche clients. Requirements At least 2 years of project and/or clinical trial coordinator/management experience in a regulated, CRO, diagnostic, and/or pharmaceutical industry with regulated documentation exposure to clinical studies. Experience with clinical projects that require rapid activity/milestone achievement. Strong communication, collaboration, and organizational skills. Bachelor's degree required (Life Sciences preferred). Preferred Previous experience with standard project management process (PMI) desired. Experience in clinical trial management and knowledge of bio-sample (clinical testing) management and process flow. Preferred experience in clinical studies or companion diagnostics. Diagnostic and/or Pharmaceutical industry and relevant diagnostic area knowledge preferred. #J-18808-Ljbffr Jobvious