Clinical Research Associate

CRA Team Opportunity in Dallas, TexasJoin our CRA team in Dallas, Texas! The Clinical Research Associate position offers an exciting career within clinical research! For those with Life Science PhD backgrounds wanting to explore the research field, travel the US, and be part of a team bringing pharmaceutical and medical devices to market - this is the right opportunity for you!This position is office based in Dallas, Texas.Medpace CRA Training Program (PACE®)No prior research experience is needed, as Medpace provides comprehensive initial and ongoing training, unmatched by other CROs. The PACE® (Professionals Achieving CRA Excellence) Training Program includes the following:A platform to effectively and confidently carry out CRA duties to ultimately become a high-functioning, independent, Medpace CRAInteractive discussions with hands-on exercises and practicumsCore departmental rotations to learn various aspects of the drug/device development and approval processWhy CRA?Exciting travel opportunitiesMake a difference on a larger scale through the development of medical drugs and devicesDynamic working environment with varying day-to-day responsibilitiesExposure to multiple therapeutic areasDefined CRA promotion and growth ladderWe 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 moreCRA training program - PACE®Ongoing 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 complianceQualificationsMinimum of a Bachelor's degree in a health or science related field, PhD preferredAbility to travel 60-70% to locations nationwide is requiredA valid driver's license and the ability to drive to monitoring sitesMinimum 1 year healthcare-related work experience preferredProficient 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 6,000 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.Dallas PerksFlexible work environmentCompetitive PTO packages, starting at 20+ daysCompetitive compensation and benefits packageCompany-sponsored employee appreciation eventsEmployee health and wellness initiativesCommunity involvement with nonprofit organizationsStructured career paths with opportunities for professional growthDiscounts on local sports games, fitness gyms and attractionsModern, ecofriendly campus with an on-site fitness centerFree on-site parkingOutdoor seating and workspaceAwardsNamed 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.