Clinical Research Training Specialist Jobs in Texas

Follows patients on study and maintains knowledge of adverse events

Collaborates with physicians, mid-level practitioners, research nurse and data managers to document patient care

Coordinates reports for the study manager for submitting grant data in a timely manner

Provides study related coordination including protocol maintenance

Develops and maintains a processing and tracking system for all protocol related documents

Develops patient care methodology for protocols, including criteria for patient participation

Knowledge of Federal and State regulatory issues/mandates concerning Institutional Review Board requirements

This position has potential to work remotely (must live in California).

Two years’ experience with Word, Excel and Internet access/use

Previous experience with clinical research

BS/BA degree in health sciences or related field

Formal training in decision support, databases, spreadsheet, report writer, query/relational database computer software applications