Clinical Science Program Specialist | 1059399

Our Goal Treat our consultants and clients the way we would like others to treat us! Interested in joining our team? Check out the opportunity below and apply today! The Opportunity Under general supervision, the Clinical Science Program Specialist manages multiple clinical and lab services projects of less complex nature 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 pharma services plan. 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. Performs tactical coordination of timelines for all projects and functions within CDx Pharma Services and: Develops project plans, establish and coordinate 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 exchange. Guides 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 and 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 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 are required. Bachelor’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 diagnostics. Diagnostic and/or Pharmaceutical industry and relevant diagnostic area knowledge preferred. Don’t meet every single requirement? Studies have shown that women and people of color are less likely to apply to jobs unless they meet every qualification. At Revel IT, we are dedicated to building a diverse, inclusive, and authentic workplace, so if you’re excited about this role, but your experience doesn’t align perfectly with every qualification in the description, we encourage you to apply anyway. You might be the right candidate for this or our other open roles! Revel IT is an Equal Opportunity Employer. Revel IT does not discriminate on the basis of race, religion, color, sex, gender identity, sexual orientation, age, non‑disqualifying physical or mental disability, national origin, veteran status or any other basis covered by appropriate law. All employment is decided on the basis of qualifications, merit, and business need. Reference:1059399 #J-18808-Ljbffr Techlifecolumbus