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Clinical Science Program Specialist

Company: Revel IT
Location: Tucson
Posted on: March 27, 2020

Job Description:

We have a contract need for a Clinical Sciences Program Specialist in Tucson, AZ who will manage clinical and lab services projects from initiation through contract completion. Applies project management skills and experience in delivering projects on time, within budget and with high customer satisfaction. Facilitates cross-functional interactions to complete the assigned projects within the deadline and compliance with protocol. -- Responsibilities: The employee is assigned on projects that may be limited in scope and/or of low to medium complexity. It may involve collaboration with other Clinical Sciences Program Specialist Senior or Clinical Sciences Program Manager. Manages clinical testing and lab services projects from initiation through contract completion in collaboration with Specialist Senior or Program Manager. 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. Proposes options to close gaps and get projects back on track. 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 exchange. Guides and manages cross-functional interactions to complete the assigned projects within the deadline. Interface with resources outside of the company (Contract Research Organizations (CROs), site investigators, client counterparts, etc.) and serves as single point of contact with Pharma and company 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 company clients. Performs miscellaneous duties and special projects as assigned -- Requirements: Bachelor's Degree in a related field or equivalent combination of education and work experience 3 years of project and/or clinical trial coordinator/management experience 3 years of experience with projects that require rapid activity/milestone achievement Possesses problem solving skills and ability to coordinate project related activities Familiarity with management of Clinical Trials Understanding of Quality and Regulatory processes Knowledge of clinical sample process flow and testing Strong Written and verbal communication skills and meeting facilitation skills Proficiency with word processing, spreadsheet, database and email software (e.g., Microsoft Excel, Microsoft Word) Possesses interpersonal skills and ability to work in a team environment. Displays leadership skills Ability to work under time pressure while maintaining high standards of precision and data quality Ability to manage projects with activity/milestone achievement to complete clinical study testing and data reporting to pharma partners Ability to apply specialized knowledge and skills in the functional areas, particularly interfacing with laboratory, scientific, and medical staff -- Preferred: Master's Degree in a related field Specific Project Management Training, or Clinical Research training and/or certification Experience in clinical trial management and knowledge of bio-sample (clinical testing) management and process flow preferred Previous experience with standard project management process (PMI) desired Diagnostic and/or Pharmaceutical industry and relevant diagnostic area knowledge preferred

Keywords: Revel IT, Tucson , Clinical Science Program Specialist, Healthcare , Tucson, Arizona

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