Clinical Research Associate - PhD in Life Sciences

Job SummaryJoin 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 opportunities Make a difference on a larger scale through the development of medical drugs and devices Dynamic working environment with varying day-to-day responsibilitiesExposure to multiple therapeutic areasDefined CRA promotion and growth ladder 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 moreCRA training program - PACEOngoing 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) 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 Please note benefits may vary based on country. What 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