Job details
Salary $85 - $95 an hour job type contract
Full job description
Description:
Looking for an experienced project managerAt least three plus years of experience with 3-5 years of vendor/cro managementConsultant needs to fully understand clinical trial process and be able to run trials independently.
Therapeutic areas we`re looking for are as follows: diabetes (t1 and t2 a nice to have) cardiovascular indications critical care – icu experience metabolic rare diseases cell or gene therapy medical devicePosition is fully remote.
Skills:
Project management, clinical project management
Additional skills & qualifications:
Responsible for the overall coordination and management of clinical trials from start up through close out activitiesDirects the technical and operational aspects of the projects, securing the successful completion of clinical trialsWorks with major functional area leads to identify and evaluate fundamental issues on the project, interpret data on complex issues, makes sound business decisions and ensure solutions are implementedWorks to ensure all project deliverables meet the customer’s time/quality/cost expectationsAccountable for ensuring all project deliverables meet the customer/contract expectations, providing accurate hour forecasts, reviewing pass-through costs and ensuring timely invoicing with the support of project management directors and/or associate directors while working in collaboration with other functional area leadsMay work with directors and/or associate directors, project management and contracts & proposals development on the development of new proposals and general capabilities presentations to customers for new business.
Manages allocated studies according to timelines and quality standardsCoordinates activities of all functional departments and vendors involved in the projectWorks with team and management to develop plans/guidelines for project implementation using ppd toolsMonitors and analyzes project status to ensure successful completion of project parameters, milestones, timetables (i.e., regulatory document, research agreement, site payments, interim monitoring, crf retrieval, crf data entry, etc.)Ensures teams are entering and updating internal tracking tools e.gProject pulse, cascade, etcWorks with team to identify potential risks, develop contingency plans.
Acts as principal liaison between sponsor and ppd by facilitating the flow of information between ppd and clientProvides sponsor with timely project updates, project related fiscal information, ensures correct protocol interpretations, and obtains
Please reach out to michael silberman at (612) 655-7633 for further inquiry.
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