Clinical Research Coordinator

Overview

• Coordinate and oversee clinical trials, ensuring compliance with protocols and ethical standards.
• Collaborate with multidisciplinary teams to ensure smooth execution of research studies.
• Support study start-up, enrollment, and closeout processes effectively.
• Maintain accurate research records, including case report forms and drug dispensation logs.
• Monitor participant adherence to study protocols and administer questionnaires.
• Ensure proper specimen collection, labeling, storage, and transport.
• Analyze research data and compile reports on study outcomes.
• Manage logistics and maintain inventory of necessary equipment and supplies.

Key Responsibilities & Duties

• Monitor health of study participants and ensure adherence to study rules.
• Recruit, interview, screen, enroll, and randomize study subjects.
• Obtain informed consent and collect medical histories from participants.
• Conduct study visits and maintain source documentation accurately.
• Resolve queries and document adverse events or protocol deviations.
• Liaise with laboratories and ensure compliance with regulatory requirements.
• Perform clinical tasks such as phlebotomy, vital signs monitoring, and ECG administration.
• Coordinate stipend payments and manage study-related finances.

Job Requirements

• Bachelor's degree in a health-related field is preferred.
• Minimum of 2 years of on-site clinical research experience with patients.
• Proficiency in study start-up, enrollment, and closeout processes.
• Experience with regulatory filing, accessing documents, and study submissions.
• Strong skills in subject interaction, including recruitment and informed consent.
• Competency in clinical tasks such as phlebotomy, vital signs, and ECG.
• Ability to manage administrative tasks, including source documentation and query resolution.
• Knowledge of ethical standards and regulatory compliance in clinical research.