Experienced regional Clinical Research Associates to support clinical trials in multiple therapeutic areas. 

Long-term, open-ended opportunities for  CRAs with 50% – 75% availability in Miami, Florida; Orlando, Florida; and New Jersey.

Responsibilities include: Monitoring and managing clinical trials for medical devices, pharmaceuticals and in-vitro diagnostics.  Participating in site selection, initiation, training, monitoring, troubleshooting and closure activities.  Assisting in the development of protocols and CRFs.  Reviewing regulatory documents.  Writing and submitting reports of site findings and other activities to ensure study goals are met.

Requirements include: BA/BS, and/or equivalent work experience required. Degree in science/health related field (e.g., nursing, biology, biomedical, etc.) preferred.  At least 5 years of complex therapeutic experience.  Knowledge of Good Clinical Practices (GCP) and applicable FDA regulations expected.  Position may require travel.