Clinical Research Coordinator

Overview

• Coordinate and oversee clinical trials, ensuring smooth execution and adherence to protocols.
• Support data collection, analysis, and reporting for research studies.
• Communicate with study participants, administering questionnaires and monitoring adherence.
• Collaborate with laboratories and ensure compliance with ethical standards.
• Maintain accurate research records and manage specimen logistics.
• Ensure availability and functionality of necessary equipment and supplies.
• Provide support for regulatory filing, study submissions, and finance-related tasks.
• Engage in participant recruitment, screening, and enrollment activities.

Key Responsibilities & Duties

• Monitor health and adherence of study participants throughout trials.
• Compile reports summarizing trial outcomes and effectiveness of procedures.
• Administer informed consent and collect medical histories from participants.
• Conduct study visits and address protocol deviations.
• Perform clinical tasks including phlebotomy, vital signs monitoring, and ECGs.
• Resolve queries and document adverse events or protocol deviations.
• Order and manage study supplies and equipment.
• Ensure compliance with regulatory requirements and ethical standards.

Job Requirements

• Bachelor's degree in a health-related field preferred.
• Minimum of 2 years of clinical research experience; oncology experience required.
• Proficiency in regulatory filing, study submissions, and query resolution.
• Strong clinical skills including phlebotomy, vital signs, and ECG monitoring.
• Experience in participant recruitment, screening, and enrollment.
• Fluency in Spanish is mandatory for effective communication.
• Ability to work on-site full-time and manage multiple trials simultaneously.
• Knowledge of ethical standards and regulatory compliance in clinical research.