Clinical Research Associate – Cincinnati, OH (Entry-Level)

About the positionResponsibilitiesConduct qualification, initiation, monitoring, and closeout visits at research sites in compliance with the approved protocol. Communicate with medical site staff including coordinators and clinical research physicians. Verify adequate investigator qualifications, training, and resources, including facilities and staff. Perform medical record and research source documentation verification against case report form data. Conduct on-site and virtual monitoring activities with a risk-based approach.Ensure the investigator is enrolling only eligible subjects. Review regulatory documents and ensure compliance with protocols. Manage medical device and investigational product accountability and inventory. Verify and review adverse events and ensure accurate data reporting. Assess patient recruitment and retention success and suggest improvements. Complete monitoring reports and follow-up letters summarizing findings and recommended actions. RequirementsBachelor's degree in a health or science-related field; advanced degrees or prior clinical research experience is a plus.Ability to travel 60-70% to locations nationwide. Valid driver's license and ability to drive to monitoring sites. Proficient knowledge of Microsoft® Office. Strong communication and presentation skills. Detail-oriented and efficient in time management. Nice-to-havesAdvanced degrees in health or science-related fields. Prior clinical research experience. BenefitsCompetitive travel bonusEquity/Stock Option ProgramTraining completion and retention bonusAnnual merit increases401K matchingOpportunity to work from homeFlexible work hoursHome office furniture allowanceIn-house travel agents and reimbursement for airline clubOpportunities for leadership positionsOngoing therapeutic training by in-house physiciansIn-house administrative support for CRAsOpportunities to work with an international team of CRAs.Apply tot his job