Home-Based Experienced CRA (Clinical Research Associate)- Bonus/Equity

Home-Based Experienced CRA (Clinical Research Associate)- Bonus/EquityJoin to apply for the Home-Based Experienced CRA (Clinical Research Associate)- Bonus/Equity role at Medpace.Experienced 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-size CRO that is focused on full-service project work. Through our fast PACE Training Program, you will receive customized, expedited training, and efficient onboarding to familiarize you with Medpace systems.We offer the following:Competitive travel bonusEquity/Stock Option program for high performing CRAsAnnual merit increases401(k) matchingThe opportunity 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, and TSA pre-checkOpportunity for leadership positions/career advancement – Lead CRA, CRA Manager, Clinical Trial Manager, Training and Development ManagerCustomized Fast PACE training program based on your experience, therapeutic background, and interestUser friendly CTMS with electronic submission and approval of monitoring visit reportsOngoing therapeutic training by our in-house physicians who are medical and regulatory expertsIn-house administrative support for all levels of CRAsOpportunities to work with international team of CRAsMany additional perks unmatched by other CROsResponsibilitiesConduct qualification, initiation, monitoring, and closeout visits at research sites in compliance with the approved protocolCommunicate 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 that 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 nationwideMust have a minimum 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 managementMedpace OverviewMedpace 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 us 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.Cincinnati PerksCincinnati Campus OverviewFlexible work environmentCompetitive PTO packages, starting at 20+ daysCompetitive compensation and benefits packageCompany-sponsored employee appreciation eventsEmployee health and wellness initiativesCommunity involvement with local nonprofit organizationsDiscounts on local sports games, fitness gyms and attractionsModern, eco-friendly campus with an on-site fitness centerStructured career paths with opportunities for professional growthDiscounted tuition for UC online programsAwardsNamed a Top Workplace in 2024 by The Cincinnati EnquirerRecognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibilityWhat to Expect NextA Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.Seniority level: Not applicableEmployment type: Full-timeJob function: Research, Analyst, and Information TechnologyIndustries: Pharmaceutical ManufacturingJ-18808-Ljbffr