Clinical Research Coordinator I, II, or III

Key Responsibilities

• Lead the coordination of clinical studies and execute ongoing follow-up visits, ensuring strict compliance with protocols, SOPs, and GCP guidelines.
• Manage daily operational tasks such as document review, data entry, preparation of test materials, and collection of clinical data.
• Organize and conduct pre-study meetings and respond to queries from Quality Assurance and Statistics departments.
• Prepare and maintain all study documentation including protocol amendments, case report forms, and study-specific documents.
• Cover proper adherence to safety, quality management, and laboratory practices in all aspects of study operation.
• Address and resolve issues with panelists, arrange project work, and assist with additional tasks as assigned by leadership.

Qualifications & Requirements

• Associate Degree or at least 2 years of relevant experience with a GED or High School Diploma.
• Understanding of clinical research concepts and willingness to learn new processes.
• Ability to handle multiple projects and work efficiently in a highly professional setting.
• Strong organizational, communication, and problem-solving skills.
• Basic computer proficiency.
• Fit for Duty medical assessment required.
• No supervisory responsibilities.
• No travel required.
• Work is performed in a controlled, indoor environment with no exposure to hazardous conditions.