Clinical Research Coordinator

Overview

• Coordinate and oversee clinical trials, ensuring smooth execution and adherence to protocols and ethical standards.
• Collaborate with research teams to manage study logistics, participant interactions, and regulatory compliance.
• Monitor participant health and adherence to study rules, administering questionnaires and collecting medical history.
• Analyze and compile research data, preparing reports on trial outcomes and findings.
• Maintain accurate research records, including case report forms and drug dispensation documentation.
• Ensure availability and functionality of necessary equipment and supplies for trials.
• Work closely with laboratories and other stakeholders to ensure protocol compliance.

Key Responsibilities & Duties

• Coordinate study start-up, enrollment, and closeout activities for clinical trials.
• Recruit, screen, and enroll study participants, obtaining informed consent and conducting study visits.
• Monitor participant health, adherence to protocols, and administer questionnaires.
• Collect and analyze research data, resolving queries and addressing protocol deviations.
• Maintain accurate and organized research records, including source documentation and EDC entries.
• Perform clinical tasks such as phlebotomy, vital signs monitoring, and ECG administration.
• Ensure compliance with regulatory requirements and ethical standards throughout the study.
• Manage logistics, including ordering supplies and ensuring equipment functionality.

Job Requirements

• Bachelor’s degree in a health-related field is preferred.
• Minimum of 2 years of on-site clinical research experience directly involving patient interaction.
• Proficiency in study start-up, enrollment, and closeout processes.
• Experience with regulatory filing, stipend payments, and subject interaction tasks.
• Clinical skills including phlebotomy, vital signs monitoring, and ECG administration.
• Strong organizational skills for maintaining accurate research records and addressing protocol deviations.
• Ability to work on-site and collaborate effectively with teams and laboratories.
• Knowledge of ethical standards and regulatory compliance in clinical research.