Clinical Science Program Specialist

Clinical Science Program Specialist

Location: Onsite in Tucson, AZ

Pay Rate: $35/hour

1 year contract with potential for extension and/or permanent placement

Weekly pay and healthcare benefits offered!

The Opportunit

• yManages 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
• .Performs tactical coordination of timelines for all projects and functions within CDx Pharma Services and
• :- Develops project plans, establish 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 challenge assumptions
• .Oversees and guides day to day activities of sample process flow and accurate reporting of results
• .Implements / pulls in best practices within the clinical sciences team; fosters continuous improvement by ensuring knowledge and experience exchang
• eGuides and manages cross-functional interactions to complete the assigned projects within the deadline
• .Interfaces with resources outside of the company (Contract Research Organizations (CROs), site investigators, client counterparts, etc.) and serves as single point of contact with Pharma 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 clients

. Qualifications

• At least 2 years of project and/or clinical trial coordinator/management experience in a regulated, CRO, diagnostic, and/or pharmaceutical industry with regulated documentatio
• nExposure to clinical studie
• sExperience with clinical projects that require rapid activity/milestone achievement
• .Strong communication, collaboration, and organizational skills are require
• dBachelor's degree is required (Life Sciences is 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
• .Preferred experience in clinical studies or companion diagnostic
• sDiagnostic and/or Pharmaceutical industry and relevant diagnostic area knowledge preferred