Job Summary

• The Clinical Research Coordinator performs clinical research activities, investigations, and develops and compiles reports based on records, observations, test results and other information received for the purpose of advancing knowledge through clinical trial research in multiple disciplines.
• This role ensures timely and accurate reporting of adverse events, and helps maintain study budgets, supplies, and regulatory documentation.
• Recruits and screens clinical research patients for protocol eligibility, obtains informed consent through patient education, and serves as a resource to physicians concerning protocol requirements.

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Skills & Requirements

Key Requirements

• Minimum 2 years related experience
• Bachelor's degree preferred
• Certified Clinical Research Professional preferred

Work Rights