Clinical Research Coordinator II - FT - Days - OHR

Responsibilities

• Coordinates and assists with the implementation of multiple clinical research studies.
• Responsible for training and educating staff.
• Collaborates to ensure the compliance with local, state and federal regulations and standards.
• Assists with responding to and preparing for audits and participates in audits.
• Processes and ships research specimens per protocol guidelines.
• Manages the handling of adverse events, compliance and other participant-related issues.
• Handles resolution of data queries with sponsor.
• Completes, organizes, and submits Institutional Review Board (IRB) for phase 1 - 4 trials required by the sponsor.
• Conducts initiation, monitoring and close out visits with the sponsor.
• Assists in training/mentoring of CRC I and other team members as required.

Qualifications

• Two (2) years of clinical research experience required.

Competencies

• ACCOUNTABILITY
• ACCURACY
• Clinical Research - Regulatory Compliance
• CUSTOMER SERVICE
• DEVELOPS RELATIONSHIPS
• EFFECTIVE COMMUNICATION
• RESEARCH - REPORTING
• RESPONDING TO CHANGE
• STANDARDS OF BEHAVIOR

Education and Certification Requirements

• A high school diploma or equivalent is required.