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 PACE® Training Program, you will join other Professionals Achieving CRA Excellence and receive customized, expedited training, and efficient onboarding to familiarize experienced CRAs with Medpace systems.
Responsibilities Verify that the rights and well-being of subjects are protected, the reported trial data are accurate, complete, and verifiable from source documents, and the conduct of the trial is in compliance with the currently approved protocol/amendment(s), GCP, and applicable regulatory requirement(s);Ensure site compliance while conducting qualification, study initiation, routine monitoring, and study site close-out visits for research sites according to Medpace/Sponsor Standard Operating Procedures (SOPs);Serve as the primary resource to the clinical investigator and site staff;Maintain close collaboration, interaction, and effective working relationships with Medpace internal cross-functional teams;Ensure quality completion of visit reports, follow-up letters, and maintenance of study-related databases and ClinTrak ® Monitoring Portal; andMust have and maintain a valid driver’s license and the ability to drive to monitoring sites. This specifically applies in the US, Canada, any countries where cars/car allowance are provided by Medpace, and other countries dependent on monitoring travel and patterns as designated by Medpace. Qualifications Bachelor's degree with at least 2-4 years of Experience as a Clinical Research Associate;Must have a minimum of a bachelor’s degree in a health or science related field;Proficient knowledge of Microsoft® Office;Outstanding communication skills; andMust be detail-oriented and efficient in time managementDemonstrated ability to independently function as a Lead CRA (on more complex studies as applicable), including the ability to effectively plan, delegate, and review the work of others;Demonstrated ability to present at meetings, including the ability to seek, make, and develop suggestions; andKnowledgeable enough about Clinical Monitoring practices and procedures to represent the function in internal and external (e.g., business development) meetings. 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?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.
Medpace Perks
Flexible work environment Competitive compensation and benefits packageCompetitive PTO packagesStructured career paths with opportunities for professional growthCompany-sponsored employee appreciation events Employee health and wellness initiativesAwards
Recognized 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 compatibility
What to Expect Next
A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.
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