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Medpace Networking Event at University of Kentucky (upcoming grads) Job Locations United States-OH-Cincinnati Category Medpace Recruitment Events Job Summary Medpace will be hosting an In-Person Networking Event at the University of Kentucky for upcoming graduates! Due to the scientific nature of our business this event will be focusing on top candidates with life sciences backgrounds. WHEN: April 4th at 5:30 PM EST WHERE: Lexington, KY More details regarding the format of this virtual event will be provided should you be selected to attend* Responsibilities Below are the positions we will be recruiting for at this event: Clinical Research Associate Comprehensive training program that provides resources and knowledge to monitor sites independently Travel to non-local, national study sites 60-80% of the time Communicate with medical staff and clinical research physicians on site Project Coordinator - CRO Partner with Clinical Trial Manager to coordinate daily study activities Central point of contact for internal and external team members Create and maintain project timeline Project Coordinator - MRL Create and maintain laboratory manuals (general and study-specific) and other study- related documents; Develop and present clinical laboratory presentations at investigator meetings; Design specifications and monitor production of specimen collection kits Project Coordinator - Independent Data Monitoring Partner with the Independent Data Monitoring Manager to identify and contract independent physicians and industry experts to assemble Data Monitoring Committees (DMCs) to review of safety and efficacy data for ongoing trials Provide administrative, logistical, and coordinating support for DMCs (including scheduling meetings, distributing unblinded data, and documenting decisions and outcomes) Assist in the development and maintenance of study specific documents describing DMC processes and procedures Feasibility Coordinator Coordinate feasibility assessments and deliver high quality, accurate feasibility data to internal and external teams; Develop preliminary proposal strategy for site and country selection; Present feasibility results to members of the proposal team to assure correct assumptions were implied and strategy is in line with our therapeutic and operational experience Patient Recruitment Coordinator Implement various recruitment strategies for clinical research studies; Work with the sites, CTM and Clinical Research Associate to discuss recruitment strategies and enrollment targets; Develop recruitment plans and ideas for new and on-going studies Regulatory Submissions Coordinator Communicate with research sites (doctor's offices, universities, hospitals, etc.) to collect all essential documents required before the site begins to screen patients to participate in the clinical trial; Maintain and perform ongoing quality review of trial documents within the Trial Master File (TMF); Collect, review, organize, and assemble regulatory start-up submissions (includes submissions to Institutional Review Boards) Data Standard Analyst Implement edit check specifications via SAS programming to assist with reconciliation of data discrepancies; Create annotated CRFs and mapping specifications per CDISC SDTM standards; Create SDTM data via SAS programming by implementing data standards for collected study level source data Clinical Packaging and Supplies Specialist Support and collaborate in all activities related to investigational supply chain; Support CP&S department to translate clinical study protocol into investigational supply chain; Monitor alignment of CP&S timelines with project timelines