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.