Clinical Research Coordinator

Overview

• Coordinate and manage clinical trials to ensure smooth execution and compliance with protocols.
• Monitor study participants’ health and adherence to study rules throughout the trial process.
• Analyze and compile research data to evaluate the effectiveness of medical procedures and technologies.
• Collaborate with laboratories and regulatory bodies to ensure ethical and regulatory compliance.
• Maintain accurate research records, including case report forms and drug dispensation documentation.
• Facilitate participant interaction, including recruitment, informed consent, and administering questionnaires.
• Ensure availability and functionality of necessary equipment and supplies for research studies.

Key Responsibilities & Duties

• Oversee 3-4 clinical trials, ensuring adherence to protocols and ethical standards.
• Collect and analyze research data to support study objectives and outcomes.
• Recruit, screen, and enroll study participants, obtaining informed consent and medical history.
• Monitor participant adherence to study rules and document adverse events or protocol deviations.
• Maintain source documentation and electronic data capture systems, resolving queries as needed.
• Perform clinical tasks such as phlebotomy, vital signs monitoring, and ECG administration.
• Coordinate logistics, including specimen collection, labeling, storage, and transport.

Job Requirements

• Bachelor’s degree in a health-related field is preferred.
• Minimum of 2 years of on-site clinical research experience with direct patient interaction.
• Proficiency in study start-up, enrollment, and closeout processes.
• Experience with regulatory filing, stipend payments, and subject interaction.
• Competence in clinical skills such as phlebotomy, vital signs monitoring, and ECG administration.
• Strong organizational and communication skills to manage multiple trials effectively.
• Ability to maintain accurate records and ensure compliance with ethical and regulatory standards.