Entry-level Clinical Research Associate
Core
Conduct on-site monitoring visits to ensure clinical trial compliance, verify data accuracy, and manage investigational product accountability for drug and medical device development.
Role type
Entry-level Clinical Research Associate (CRA)
Builds
Clinical trials for pharmaceuticals and medical devices
Domain
Clinical research / Biopharma
Required skills
Site monitoring, regulatory document review, medical record verification, adverse event reporting, patient recruitment assessment, inventory management
Preferred skills
Healthcare work experience, travel adaptability, detail-oriented documentation (via careerplan.io/jobs/12235-entry-level-clinical-research-associate-at-medpace)
Technologies
Clinical Trial Management System (CTMS), Electronic Data Capture (EDC)
Responsibilities
Conduct qualification, initiation, monitoring, and closeout visits; Verify investigator qualifications and site resources; Review regulatory documents and verify subject eligibility; Monitor adverse events and concomitant medications; Assess patient recruitment and retention; Complete monitoring reports and follow-up letters.
Seniority
Entry-level, training-focused IC