Regional Clinical Research Associate

Overview:

The CRA / Sr. CRA monitors activities at clinical study sites to assure adherence to Good Clinical Practices (GCPs), SOPs, and study protocols. Will review regulatory documents as required and prepare site visit reports. Responsible for multiple projects and must work both independently and in a team environment. May participate in the study development and start-up process including reviewing protocols, designing and/or reviewing CRFs, preparing Informed Consent forms, developing study documents, organizing and presenting at investigator meetings, working with management on monitoring strategy, and/or developing project-specific CRA training.

Requirements:

- Bachelors degree (BS, BA, or RN equivalent) in a biological or science-related field is preferred
- Minimum of five to six years of clinical experience in the pharmaceutical, biotechnology, or CRO industry
- CNS experience preferred
- Ability to travel up to 40%
- Familiar with various EDC systems including INFORM
- Excellent written and verbal communication skills

To find out more about Real Staffing please visit www.realstaffing.com