Minimum of 2 years of experience as a Clinical Research Coordinator (CRC), preferably in a clinical or oncology research setting.
Demonstrated experience in clinical research, including screening and pre-screening patients, chart review, and patient recruitment.
Proficiency in obtaining informed consent and explaining clinical trial procedures and requirements to patients in a clear and compassionate manner.
Strong skills in source documentation, ensuring accurate, complete, and timely recording of all study-related information.
Ability to work effectively in a patient-facing role within a busy clinic environment, spending significant time in direct interaction with patients and clinical staff.
Experience with oncology clinical trials or oncology clinical studies, including familiarity with complex protocols and therapy-related procedures.
Capability to manage multiple trials simultaneously, overseeing core coordination responsibilities while providing backup support on additional studies.
Competence in using electronic medical records (EMR) for documenting research activities and coordinating patient care.
Attention to detail and strong organizational skills to ensure protocol compliance, proper scheduling, and adherence to study timelines.
Ability to collaborate with nurses, medical assistants, infusion staff, and other clinical professionals in a multidisciplinary team.
Enthusiastic, positive attitude and strong interpersonal skills to build rapport with patients and colleagues and contribute to a supportive research environment.
Knowledge of protocol-driven scheduling for procedures such as EKGs, vitals, and other diagnostic or monitoring tests.
Understanding of quality control processes in clinical research, including data verification and compliance checks.
