Experienced Clinical Research Associate - Home-Based

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 ProfessionalsAchieving CRA Excellence and receive customized, expedited training, and efficient onboarding to familiarize experienced CRAs with Medpace systems.

• 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; and
• Must 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.

• 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; and
• Must be detail-oriented and efficient in time management
• Demonstrated 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; and
• Knowledgeable enough about Clinical Monitoring practices and procedures to represent the function in internal and external (e.g., business development) meetings.