Clinical Research Coordinator

Clinical Research Coordinator Overview

• The Clinical Research Coordinator will oversee oncology-focused clinical trials, ensuring protocol compliance and advancing cancer research.
• Collaborate with multidisciplinary teams to manage trial operations, participant care, and data integrity effectively.
• Educate participants on study objectives, procedures, and expectations, ensuring informed consent and active engagement.
• Monitor participant health, protocol adherence, and data accuracy throughout all phases of the study.
• Facilitate laboratory work, imaging procedures, and other trial-related activities with precision and efficiency.
• Maintain meticulous documentation of study visits, interactions, and collected data to uphold research integrity.
• Ensure availability and functionality of necessary equipment and supplies for seamless trial execution.
• Contribute to the advancement of oncology research and the improvement of patient outcomes through dedicated coordination efforts.

Clinical Research Coordinator Key Responsibilities & Duties

• Screen, enroll, and schedule participants, ensuring informed consent and accurate medical history collection.
• Conduct study visits, monitor adherence, and manage adverse events with precision and care.
• Coordinate with labs, imaging vendors, pharmacy staff, and infusion teams for seamless trial execution.
• Prepare and submit study documentation, addressing protocol deviations and reporting to IRB as required.
• Manage specimen collection, labeling, packaging, and storage processes efficiently and accurately.
• Ensure compliance with regulatory standards and ethical guidelines throughout all trial phases.
• Maintain and organize lab kits, medical records, and corresponding reports meticulously.
• Collaborate with teams to ensure smooth trial operations and participant satisfaction.

Clinical Research Coordinator Job Requirements

• Bachelor's degree in a health-related field, preferably in science or medical studies.
• Minimum of 3 years of clinical research experience, ideally in oncology trials.
• Phlebotomy certification preferred; proficiency in vital signs, EKG, and lab kit management.
• Strong knowledge of medical terminology and clinical trial protocols essential.
• Proficiency in EMR and EDC systems for accurate data management.
• Exceptional organizational skills to maintain detailed records and manage supplies.
• Effective communication skills for participant education and team collaboration.
• Commitment to advancing oncology research and improving patient care outcomes.