Clinical Research Associate

Role:

Clinical Research Associate (CRA) - C
Location:

San Diego, CA 92121
Duration:

7 Months on W2
Shift Timings:

8 AM to 5 PM
Job Description

Member of the clinical team responsible for conducting Phase I-IV single or multi center studies according to Federal Regulations and ICH guidelines.
Responsible for assisting senior staff in planning study conduct, designing case report forms (CRFs), Contract Research Organization (CRO) selection and management, selection and training of investigator sites, planning and running study meetings, evaluation, selection and training of new study investigators, and writing and assembling submissions.
Responsible for writing basic study protocols, monitoring or overseeing monitoring of investigational sites to ensure protocol adherence, assuring timely enrollment of patients and retrieval of CRFs from study sites, processing CRFs including data cleanup and classification of data, and completion of study summary.
5+ Years' Experience Level.
Requirements

ONSITE POSITION - MUST BE LOCAL TO SAN DIEGO
5 years CRA Experience
Must be able to work onsite (San Diego)
Travel can be up to 30% (mostly CA but could be other locations as well)
Science Degree
Previous Site Monitoring Experience; prefers candidate to have Medical Device or Pharmaceutical Background
Good communication and organizational skills plus detail-oriented
Please note when submitting candidates that they must be local to the San Diego, CA area. This is an onsite role, and candidates should not require relocation unless they are moving closer from within the area.

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