Clinical Research Associate

Participates in the design, administration and monitoring of clinical trials.

Responsibilities:

• Plans, organizes, performs and monitors daily project protocols.
• Collects, prepares and maintains required research documentation, such as informed consent records, case records, clinical notes and medical reports.
• Reports and assists with the management of protocol deviations, adverse events and other project-related issues.
• Assists with the preparation and delivery of internal and external presentations, conference reports and lectures, and publishing submissions.
• Understanding of the Food and Drug Administration (FDA) rules is beneficial.