Job SummaryExperienced Clinical Research Associate (CRA) - join our growing team!Medpace is growing quickly and we are seeking experienced Clinical Research Associates to join our team. We are an innovative, scientifically oriented, mid-sized CRO focused on full-service project work. Through our expedited PACE Training Program, you will receive customized training and efficient onboarding to familiarize yourself with Medpace systems.We Offer the Following: Competitive travel bonusEquity/Stock option programTraining completion and retention bonusAnnual merit increases401K matchingOpportunity to work from homeFlexible work hours across days within a weekRetain airline reward miles and hotel reward pointsHome office furniture allowance, laptop, mobile phone with hotspot for internet access anywhereIn-house travel agents, reimbursement for airline club membership, and TSA pre-checkOpportunity for leadership positions – Lead CRA, CRA Manager, Training and Development Manager, and many moreUser friendly CTMS with electronic submission and approval of monitoring visit reports;Customized, expedited PACE training program based on your experience, therapeutic background, and interestOngoing therapeutic training by our in-house physicians who are medical and regulatory expertsIn-house administrative support for all levels of CRAOpportunity to work with international team of CRAsResponsibilitiesConduct qualification, initiation, monitoring, and closeout visits at research sites in compliance with the approved protocolCommunication with the medical site staff including coordinators, clinical research physicians, and their site staffVerify adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staffMedical record and research source documentation verification against case report form data, including informing the site staff of any entry errors, ensuring good documentation practices are being adhered to and communicating protocol deviations appropriately per SOPs, GCP, and applicable regulatory requirementsOn-site and virtual/remote monitoring activities with a risk-based monitoring approach (including centralized data review) through our integrated Clinical Trial Management System to identify site deviations/deficiencies and corrective/preventive actions to bring a site back into compliance and mitigate risks moving forwardVerification the investigator is enrolling only eligible subjectsRegulatory document reviewMedical device and/or investigational product/drug accountability and inventoryVerification and review of adverse events, serious adverse events, concomitant medications and corresponding illnesses to confirm accurate data reporting in accordance with the protocolAssess the clinical research site’s patient recruitment and retention success and offering suggestions for improvementCompletion of monitoring reports and follow-up letters, which includes providing summaries of the significant findings, deviations, deficiencies, and recommended actions to secure complianceQualificationsClinical Research Associate Experience (minimum 1 year)Ability to travel 60-70% to locations nationwide is requiredMinimum of a bachelor’s degree in a health or science related fieldProficient knowledge of Microsoft OfficeStrong communication and presentation skillsDetail-oriented and efficient in time management#LI-Remote Medpace OverviewMedpace is a full-service clinical contract research organization (CRO) providing phase l-lV 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 the advancement of clinical research. We leverage in-country regulatory and therapeutic expertise across all major therapeutic areas including oncology, cardiology, metabolic, endocrinology, central nervous system, and anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, we employ more than 6,500 people across 40+ countries.Why Medpace?When you join Medpace, you become part of an innovative team that brings cutting-edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross-functional collaboration.Purpose-Driven WorkWork alongside physicians, scientists, and industry-leading experts committed to advancing the global development of medical therapeutics through clinical research excellenceCollaborative CultureContribute to an interactive team environment that empowers decision making, creative thinking, and continuous learning through open communication and mutual trust.Leadership throughout Medpace is both accessible and approachableContinuous Growth & DevelopmentOffice based environment with on-site mentorsDefined career paths with clear advancement opportunitiesIndustry renowned onboarding and training programs designed to accelerate professional developmentOngoing training and continuous learning opportunities throughout your careerAn environment that encourages employees to influence change, contribute ideas, and grow quicklyOther Employee BenefitsCompetitive compensation programs that recognize and reward performanceComprehensive health, wellness, retirement, and PTO benefitsOffice based culture with occasional WFH that provides flexibility for eligible positions after trainingCompany-sponsored social events and intramural sportsCincinnati Headquarters ExperienceA modern corporate campus designed to support collaboration and productivityMultiple on-site dining options in the heart of Madison SquareFree on-site parkingConvenient access to on-site 24-7 fitness and wellness facilitiesWhat to Expect NextA Medpace team member will review your application and if your profile matches our current needs, you will be contacted for an interview. While we review all applications carefully, we are unable to respond to every applicant, and only candidates selected for interviews will be contacted.Job SummaryCategory: Clinical Research Associate
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