Our successful Clinical Research Associates possess varied backgrounds in medical and other science-related healthcare fields. Individuals who have succeeded in the CRA role include:
NursesDieticiansPharmacy TechniciansPharmaceutical/Device Sales RepresentativesBiotech EngineersPhD/Pharm.D candidatesHealth and Wellness CoordinatorsResearch Assistants.PACE® – MEDPACE CRA TRAINING PROGRAM
No research experience is needed as Medpace provides comprehensive initial and ongoing training, unmatched by other CROs. Through our PACE® Training Program, you will join other Professionals Achieving CRA Excellence:
PACE® provides the platform to effectively and confidently carry out your duties, enhance your current abilities and ultimately help you become a high-functioning independent Medpace CRA.PACE® will prepare you by developing your CRA skills through interactive discussions and hands on job-related exercises and practicums.To supplement your in-house and field-based training you may also participate in other clinical research departmental core rotations, learning other aspects of the drug/device development and approval process.UNEXPECTED REWARDS
This role takes you on a journey through travel and excitement which will allow you to make a difference on a large scale through the enhancement of pharmaceuticals and medical devices. The CRA position provides many other distinctive advantages including:
Dynamic working environment, with varying responsibilities day-to dayExpansive experience in multiple therapeutic areasWork within a team of therapeutic and regulatory expertsDefined CRA promotion and growth ladder with potential for mentoring and management advancementsCompetitive pay and opportunity for significant travel bonusHome-based option available for CRA for more than 1 year of monitoring experience.
ResponsibilitiesAs a CRA, you will specifically be responsible for the following:
Conduct qualification, initiation, monitoring, and closeout visits for research sites in compliance with the approved protocol;Communication with the medical site staff including coordinators, clinical research physicians and their site staff;Verifying 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;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;Assessing the clinical research site’s patient recruitment and retention success and offering suggestions for improvement;Completion of monitoring reports and follow-up letters, which includes providing summaries of the significant findings, deviations, deficiencies, and recommended actions to secure compliance. Qualifications Bachelor's degree with at least 2 to 4 years of experience as a Clinical Research Associate;Willing to travel approximately 60-80% nationally;Familiarity with Microsoft® Office; andStrong communication and presentation skills a plus. Medpace 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?When you join Medpace, you become part of a team dedicated to supporting the development of ground-breaking drugs and devices. Our employees provide hope for those living with debilitating diseases. We invite you to be a part of something that is impacting millions of people around the globe while enjoying a competitive total compensation and benefits package and internal growth opportunities.
Organic Growth: Medpace is continuing to grow in all areas globally and has built an expansive research campus at its headquarters in Cincinnati, OH. In 2020, Medpace opened a new seven story building that is approximately 250,000 SQFT. In total, the headquarter's campus includes five buildings and approximately 600,000 SQFT. The company also has expanding office locations in Dallas, TX and Denver, CO.
Perks (vary by location and position):
On-site fitness center(s)Campus walking pathsCompany-sponsored social and wellness eventsOfficial Sponsor of FC CincinnatiHybrid work-from-home options and flexible work scheduleOn-site Market PlaceFree and covered parkingDiscounts for local businessesOn campus restaurants and banks coming soon
Awards:
Medpace historically named a Top Cincinnati Workplace by the Cincinnati EnquirerRecognized by Forbes as one of America's Best Mid-size Companies in 2021Medpace ranks amongst top CROs for site ratings across all 10 important attributes including CRA training, preparation & organization, accessibility of staff, open communication, and ensuring timely drug availabilityContinually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibilityRanked in the top 10 on the 2021 LinkedIn Top Companies list in CincinnatiWhat to Expect Next:
A member of our recruitment team will review your qualifications and, if interested, you will be contacted for an interview.
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