Home-Based Experienced CRA (Clinical Research Associate)- Bonus/EquityJob LocationsUnited States-OH-Cincinnati | United States-TX-Irving (Dallas) | United States-Miami | United States-TN-Nashville | United States-PA-Philadelphia | United States-IL-Chicago | United States-MO-St. Louis | United States-TN-Nashville | United States-MA-Boston | United States-MI-Detroit | United States-UT-Salt Lake City | ...CategoryClinical Research AssociateJob 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 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.Sign-On Bonus EligibleWE OFFER THE FOLLOWING:Competitive travel bonus;Equity/Stock Option program for high performing CRAs;Annual merit increases;401K matching;The opportunity to work from home;Flexible work hours across days within a week;Retain airline reward miles and hotel reward points;Home office furniture allowance, laptop, mobile phone with hotspot for internet access anywhere;In-house travel agents, reimbursement for airline club, and TSA pre-check;Opportunity for leadership positions/career advancement - Lead CRA, CRA Manager, Clinical Trial Manager, Training and Development Manager;Customized Fast PACE training program based on your experience, therapeutic background, and interest;User friendly CTMS with electronic submission and approval of monitoring visit reports;Ongoing therapeutic training by our in-house physicians who are medical and regulatory experts;In-house administrative support for all levels of CRAs;Opportunities to work with international team of CRAs; andMany additional perks unmatched by other CROs!ResponsibilitiesConduct qualification, initiation, monitoring, and closeout visits at research sites in compliance with the approved protocol;Communication with the medical site staff including coordinators, clinical research physicians, and their site staff;Verify adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staff;Medical 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 requirements;On-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 forward;Verification that the investigator is enrolling only eligible subjects;Regulatory document review;Medical device and/or investigational product/drug accountability and inventory;Verification and review of adverse events, serious adverse events, concomitant medications and corresponding illnesses to confirm accurate data reporting in accordance with the protocol;Assess the clinical research site's patient recruitment and retention success and offering suggestions for improvement; andCompletion of monitoring reports and follow-up letters, which includes providing summaries of the significant findings, deviations, deficiencies, and recommended actions to secure compliance.QualificationsClinical Research Associate Experience (minimum 1 year);A