Clinical Research Coordinator

Clinical Research Coordinator Overview

• The Clinical Research Coordinator will oversee and manage clinical trials, ensuring compliance with protocols and regulatory standards.
• Collaborate with a team to execute research studies under the guidance of the Site Operations Manager.
• Ensure smooth trial operations, including participant monitoring and data collection.
• Work on-site full-time, contributing to oncology research initiatives.
• Maintain accurate records, including case report forms and drug dispensation logs.
• Support participant recruitment, screening, and enrollment processes.
• Administer questionnaires and monitor participant adherence to study protocols.
• Ensure all necessary equipment and supplies are functional and available.

Clinical Research Coordinator Key Responsibilities & Duties

• Oversee 1-2 clinical trials, ensuring adherence to protocols and ethical standards.
• Monitor study participants’ health and compile comprehensive trial reports.
• Collect and analyze data obtained from research studies.
• Communicate study objectives and administer questionnaires to participants.
• Liaise with laboratories to ensure timely specimen processing and compliance.
• Maintain meticulous research records and manage drug dispensation documentation.
• Recruit, screen, and randomize study subjects while obtaining informed consent.
• Perform clinical tasks such as phlebotomy, vital signs monitoring, and ECGs.

Clinical Research Coordinator Job Requirements

• Associate of Science (AS) degree required; Bachelor’s degree in a health-related field preferred.
• Minimum of 2 years of clinical research experience; oncology experience preferred.
• Proficiency in regulatory filing, study submission assistance, and stipend payments.
• Strong skills in subject interaction, including recruitment, screening, and consent processes.
• Experience in source documentation, EDC query resolution, and protocol deviation management.
• Competence in clinical skills such as phlebotomy, vital signs, and ECG monitoring.
• Ability to work full-time on-site, contributing to oncology-focused research.
• Strong organizational and communication skills to ensure trial success.