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Clinical Research Opportunities- Entry Level


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Company

medpace

Description

Job Summary: The 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. ResponsibilitiesResponsible for routine departmental support including maintaining supplies, shipping, archiving, filing, faxing, scheduling meetings, and providing minutesMaintain departmental databases and electronic clinical trial registriesObtain certifications for official study documentsQualificationsBachelor's Degree in a health science fieldExcellent 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. ResponsibilitiesTrack case report formsClean the clinical database, which includes generating and resolving data clarificationsUpdate the clinical databaseReconcile clinical dataMaintain study documentationPerform QC audits of the clinical databaseQualificationsBachelor's degree in a health related field with strong attention to detail and working knowledge of Excel and Word1-2 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 documentationMaintain and perform quality review of Trial Master File (TMF)Collect, review, organize, and assemble regulatory start-up submissionsMaintain timelines for site start-upProvide advice and guidance to internal and external team members to ensure compliance with applicable regulations and requirementsReview pertinent regulations and guidance to develop proactive solutions to regulatory submissions issues and challengesQualificationsA minimum of a Bachelor's degree is required (preferably in a Life Sciences field)Some experience in an office setting is preferredExcellent organizational and prioritization skillsKnowledge of Microsoft OfficeGreat attention to detail and excellent oral and written communication skills Proposal 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 requirementsRecommend proposal and overall study strategies, based on experienceEncourage multi-disciplinary discussions among subject matter experts to facilitate full and high-quality contributions to the textEstablish timelines and deliverables and hold internal stakeholders accountable to those plans and timelinesReview 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 textCollate follow-up questions for additional information as requestedDraft standard documents in accordance with agreed strategy and Sponsor requirements within often expedited timelinesContribute to assigned process improvement initiatives and support implementationDefine action plans and timelines; manage and determine modifications needed to ensure proposal alignment with client requirements and business strategiesPerform quality control/peer review and participate in the finalization of documents and distribution to the customer and internal departments QualificationsBachelor s degree requiredStrong initiative to learnStrong written and oral communication skillsProject management skills and the ability to prioritize multiple projects and tasks Feasibility Coordinator We 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; andSupport departmental process improvement initiatives and general departmental administrative functions. QualificationsBachelors 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; andExcellent written and verbal communication skills. Medpace 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 5,000 people across 40 countries. Why Medpace?: People. Purpose. Passion. Make a Difference Tomorrow. Join Today The work we ve done over the past 30 years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future. Medpace Celebrates 30 YearsAs we celebrate 3 decades of industry expertise and organic growth, we recognize the global team responsible for driving clinical development at Medpace. Click here to learn more about Medpace Celebrating 30 Years.Cincinnati PerksCincinnati Campus OverviewHybrid work-from-home options (dependent upon position and level)Competitive PTO packages, starting at 20 days Flexible work hoursDiscounted tuition for UC online programsCompany-sponsored employee appreciation events Employee health and wellness initiatives Community involvement with local nonprofit organizationsCompetitive compensation and benefits packageStructured career paths with opportunities for professional growthPartnership and discount with onsite childcare Discounted tuition for UC online programs Discounts on local sports games, local fitness gyms and attractionsOfficial Sponsor of FC Cincinnati Modern, ecofriendly campus with an on-site fitness center, bar, and restaurants Awards:Recognized by Forbes as one of America's Best Mid-size Companies in 2021 and 2022Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility What to Expect Next:A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.
Associated topics: clinical, clinical development, clinical informatics, clinical trial, coordinator, lab, laboratory, research, research coordinator
Posted Date
01/07/2023

Listing ID
78542008
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