Clinical Research Associate (CRA) Jobs

San Diego, Ca

Clinical Research Associate

Description:
Assists in the design, planning, and implementation of clinical research projects. Coordinates activities between company, Contract Research Organizations (CRO's) and investigators to ensure compliance with protocol and overall clinical objectives. Maintains high level of professional expertise through familiarity with clinical literature and participation in project team meetings. Following instructions and discussions with Sr. Director and/or Manager, assist in designing research protocols and case report forms (CRFs), including developing procedures for the collection, verification and management of clinical data. Assist in site selection and CRO evaluation when necessary. Assess study site to ensure facility, target population and staff are adequate to support the protocol. Assist in negotiating the study budget and contract agreements.

Education/Skills Required:
BS degree in Sciences, Registered Nurse or related field. Three to five years professional experience in clinical research, nursing or the pharmaceutical industry. Good written and verbal communication skills, including public speaking; ability to establish and maintain internal and external working relationships. Ability to work independently and within a team environment. Computer literate at the intermediate level of MS Office Suite application software. Knowledge of FDA regulatory requirements (CFRs and GCPs) and internal SOPs.