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Clinical Research Opportunities- Entry Level

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OverviewMedpace is a scientifically-driven, global, full-service clinical contract research organization (CRO) providing Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Medpace's mission is to accelerate the global development of safe and effective medical therapeutics through its high-science and disciplined operating approach. We leverage local regulatory and deep therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, Medpace employs approximately 3,000 people across 36 countries.Job SummaryThe below positions are entry level roles Medpace has available:Project CoordinatorAs an Entry-Level Project Coordinator, you will have the opportunity to work within our Clinical Trial Management group, supporting our many projects and gaining some vital experience. You will be a productive member of the team, and will be mentored and supported as you develop your skills. Working directly with the clinical trial management team, you will gain valuable hands on experience to enable you to develop a career in clinical research.Responsibilities Responsible for routine departmental support including maintaining supplies, shipping, archiving, filing, faxing, scheduling meetings, and providing minutes Maintain departmental databases and electronic clinical trial registries Obtain certifications for official study documentsQualifications Bachelor's Degree in a health science field Excellent computer, organizational, and communication skillsClinical Data CoordinatorOur corporate activities are growing rapidly, and we are currently seeking a full-time, office-based Clinical Data Coordinator to join our Data Management team. This position will work on a team to accomplish tasks and projects that are instrumental to the company's success. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you.Responsibilities Track case report forms Clean the clinical database, which includes generating and resolving data clarifications Update the clinical database Reconcile clinical data Maintain study documentation Perform QC audits of the clinical databaseQualifications Bachelor's degree in a health related field with strong attention to detail and working knowledge of Excel and Word 1-2 years of experience in a pharmaceutical or CRO setting preferredRegulatory Submissions CoordinatorOur clinical activities are growing rapidly, and we are currently seeking a full-time, office-based Regulatory Submissions Coordinator to join our Clinical Operations team. This position will work on a team to accomplish tasks and projects that are instrumental to the company's success. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you.Responsibilities Communicate with research sites regarding the distribution and review of site essential documentation Maintain and perform quality review of Trial Master File (TMF) Collect, review, organize, and assemble regulatory start-up submissions Maintain timelines for site start-up Provide advice and guidance to internal and external team members to ensure compliance with applicable regulations and requirements Review pertinent regulations and guidance to develop proactive solutions to regulatory submissions issues and challengesQualifications A minimum of a Bachelor's degree is required (preferably in a Life Sciences field) Some experience in an office setting is preferred Excellent organizational and prioritization skills Knowledge of Microsoft Office Great attention to detail and excellent oral and written communication skillsProposal DeveloperWe are currently seeking a full-time, office-based Proposal Writer to join our Proposal and Feasibility team. This position will work closely with the operations and business development teams to prepare proposals for new business. If you want an exciting career where using your previous expertise and while developing and growing your career even further, this is the opportunity for you!Responsibilities May lead proposal planning meetings to: Identify issues and client requirements Recommend proposal and overall study strategies, based on experience Encourage multi-disciplinary discussions among subject matter experts to facilitate full and high-quality contributions to the text Establish timelines and deliverables and hold internal stakeholders accountable to those plans and timelines Review and analyze Request for Information (RFI) and/or Request for Proposal (RFP) documents to gain understanding of client requirements and assist in identifying missing information. Identify information to be addressed in proposal text Collate follow-up questions for additional information as requested Draft standard documents in accordance with agreed strategy and Sponsor requirements within often expedited timelines Contribute to assigned process improvement initiatives and support implementation Define action plans and timelines; manage and determine modifications needed to ensure proposal alignment with client requirements and business strategies Perform quality control/peer review and participate in the finalization of documents and distribution to the customer and internal departmentsQualifications Bachelor's degree required Strong initiative to learn Strong written and oral communication skills Project management skills and the ability to prioritize multiple projects and tasksFeasibility CoordinatorWe are currently seeking a Feasibility Coordinator, who will be a member of our global clinical operations team. By working cross functionally with our clinical operations, medical and regulatory submissions teams, as well as through obtaining direct feedback from investigative sites, this individual will provide strategic insights on country selection and enrollment planning for global clinical trials. If you are an individual with a clinical background and expertise in clinical research, please review the following career opportunity.Responsibilities Coordinate feasibility assessments and deliver high quality, accurate feasibility data to internal and external teams; Develop preliminary proposal strategy for site and country selection; Perform outreach to investigative sites to obtain indication and protocol specific feedback; 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; Create study-specific feasibility questionnaires, cover letters, and other feasibility-related documents; Assist project teams with preparation for bid defense meetings; and Support departmental process improvement initiatives and general departmental administrative functions.Qualifications Bachelors degree in life sciences required, Masters or PhD preferred; Analytical thinker with great attention to detail; Ability to prioritize multiple projects and tasks within tight timelines; Working knowledge of feasibility processes; and Excellent written and verbal communication skills.Why Medpace?When you join Medpace, you become part of a team dedicated to supporting the development of ground breaking drugs and devices. Our employees provide hope for those living with debilitating diseases. We invite you to be a part of something that is impacting millions of people around the globe while enjoying a competitive total compensation and benefits package and internal growth opportunities.Awards Medpace Named a Top Cincinnati Workplace for 2015, 2016, 2017 and 2018 by the Cincinnati Enquirer Winner of the ACRP-Avoca CRO Quality Award in 2018 Recognized with six CRO Leadership Awards from Life Science Leader magazine Eagle Award winner - which recognizes outstanding leadership, professionalism, integrity, and dedication to advancing the clinical research profession through strong site partnershipsWhat to Expect NextWe look forward to receiving your application. A member of our recruitment team will review your qualifications and if interested, you will be contacted for an interview.EO/AA Employer M/F/Disability/Vets WARNING: Please beware of phishing scams that offer opportunities with Medpace in exchange for sending money. These scammers pose as legitimate employees from actual companies. Please be advised that a Medpace employee will never ask you for a credit card, send you a check, or ask you for any type of payment as part of consideration for a role with our company. All of our careers require that you first complete an online application and go through some sort of interview process.
Associated topics: clinical, clinical development, clinical informatics, clinical trial, coordinator, lab, laboratory, research, research coordinator
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