Life Sciences Advanced Degree Hiring Event - Cincinnati
US-OH-Cincinnati
US Careers
Req #: 11417
Type: Full-Time
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Overview: Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 6,000 people across 40+ countries. Responsibilities: Below are the positions we will be recruiting for at this event: Clinical Data Coordinator: * Validate entry database designs * Report metrics and data trends on projects * Identify data conflicts and issues on projects * Work with personnel from global research sites to resolve data conflicts 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 Imaging Project Coordinator * Compile and maintain project-specific status reports and project timelines associated with Imaging studies; * Maintain inventory of imaging supplies for study sites; and * Interact with study sites and internal associates. 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 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) Associate Clinical Trial Manager (CTM) * Compile and maintain project-specific status reports within the clinical trial management system; * Interact with the internal project team, Sponsor, study sites, and third-party vendors; * Provide oversight and quality control of our internal regulatory filing system; * Provide oversight and management of study supplies; * Create and maintain project timelines; 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 applied and strategy is in line with our therapeutic and operational experience; Proposal Writer * May lead proposal planning meetings * Draft standard documents in accordance with agreed strategy and Sponsor requirements within often expedited timelines * Review and analyze Request for Proposal (RFP) and Request for Information (RFI) documents to gain understanding of client requirements and assist in identifying missing informationReview * Identify information to be addressed in proposal text * Collate follow-up questions for additional information as requestef Qualifications: * 3.3-3.5 GPA or higher * Master's or PhD in Life Sciences or related fields * Willing to work office-based in Cincinnati, OH
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