Research Coordinator

Requirements

• Identifies primary and secondary study objectives and outcome measures
• Adheres to applicable federal, state, and institutional regulations, policies, and procedures related to clinical research
• Provides timely, informative, and accurate communication with the interdisciplinary team to ensure protocol compliance and timelines of protocol-related procedures
• Identifies and intervenes to address barriers to effective informed consent discussions and decision making
• Ensures timely re-consenting as needed by the physician investigator
• Collaborates with the investigator to ascertain study patient eligibility for a clinical trial
• Evaluates patient’s adherence to and documentation of self-administered protocol agents and return of such agents
• Ensures evidence-based symptom management as permitted by the protocol

Benefits

• Comprehensive health insurance
• Retirement Plan
• Paid Time Off
• Professional Development Opportunities