Remote Clinical Project Manager

Details for the position are as follows: 5-month contract to start with the possibility of extension or conversion depending on performance and business needsRate: $35 an hourLocation: 100% Remote - Candidates may be located throughout the U.S.; however, applicants must reside in an approved hiring location. Candidates residing in the following states/territories are ineligible to apply Alabama, Alaska, Arkansas, Colorado, Delaware, Florida, Georgia, Hawaii, Iowa, Louisiana, Maryland, Mississippi, Missouri, North Carolina, Oklahoma, Pennsylvania, and Puerto Rico. Job Description: Under general supervision, 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 assigned projects within the deadline and in compliance with the Pharma Services Plan. This job is second in the Clinical Sciences project management job series, comprising four levels. The employee is assigned to 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 multiple clinical testing and lab services projects from initiation through contract completion under the supervision of the Program Manager. Acts as the 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, 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/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 assigned projects within the deadline. Interfaces with resources outside of the company, including Contract Research Organizations (CROs), site investigators, client counterparts, etc., and serves as the single point of contact with Pharma clients. Manages meeting activities such as setting agendas, organizing meeting time, and editing meeting minutes. Required Skills: Bachelor's Degree in a related field or equivalent combination of education and work experience in a related field. 2 years of project and/or clinical trial coordinator/management experience in a regulated, CRO, diagnostic, and/or pharmaceutical industry with regulated documentation. Experience in clinical trial management and knowledge of bio-sample (clinical testing) management and process flow preferred. Location Requirement: Candidates must currently reside in one of the following eligible states: Arizona, California, Connecticut, Idaho, Illinois, Indiana, Kansas, Kentucky, Maine, Massachusetts, Michigan, Minnesota, Montana, Nebraska, Nevada, New Hampshire, New Jersey, New Mexico, New York, North Dakota, Ohio, Oregon, Rhode Island, South Carolina, South Dakota, Tennessee, Texas, Utah, Vermont, Virginia, Washington, West Virginia, Wisconsin, or Wyoming. Preferred: Experience with clinical projects that require rapid activity/milestone achievement. Previous experience with standard project management process (PMI) desired. Diagnostic and/or Pharmaceutical industry and relevant diagnostic area knowledge preferred. By applying for this job, you agree to receive calls, AI-generated calls, text messages, or emails from and its affiliates, and contracted partners. Frequency varies for text messages. Message and data rates may apply. Carriers are not liable for delayed or undelivered messages. You can reply STOP to cancel and HELP for help. You can access our privacy policy at Privacy Policy