Clinical Research Coordinator - Oncology

Responsibilities

• Support the execution of Phase II–IV oncology clinical trials, including pharmaceutical-sponsored, ECOG, and investigator-initiated studies.
• Manage trials across multiple oncology disease groups, including GYN, Breast, GI/GU, Head & Neck, and Lung cancers.
• Oversee a portfolio of approximately 15–20 active clinical trials in a fast-paced, high-volume clinical environment.
• Identify and screen potential study participants using physician schedules, pathology reports, multidisciplinary tumor boards, referrals, and other clinical resources.
• Obtain informed consent and enroll eligible patients in accordance with protocol requirements and regulatory standards.
• Manage patients throughout the clinical trial lifecycle, from consent through completion of active treatment.
• Educate patients regarding study procedures, treatment schedules, and protocol requirements.
• Coincide patient care activities with physicians, infusion teams, nursing staff, radiology, pathology, laboratories, and other clinical departments.
• Maintain accurate clinical trial documentation, source records, regulatory files, patient calendars, and study-related documentation.
• Ensure compliance with study protocols, Good Clinical Practice (GCP), institutional policies, and regulatory requirements.

Qualifications

• Bachelor’s degree in health science, life science, nursing, or a related field.
• Minimum of 6 to 12 months of clinical research coordination experience supporting interventional Phase II–IV clinical trials.
• Oncology clinical trial experience is a plus (but is not required).
• Experience with patient identification, pre-screening, informed consent, enrollment, retention, regulatory compliance, and clinical data management.
• Ability to manage multiple concurrent studies while maintaining strong attention to detail and organization.
• Adaptable, solutions-oriented mindset with the ability to work effectively in a small, collaborative team environment.
• Strong interpersonal and communication skills with the ability to work closely with physicians, nurses, research staff, hospital departments, and external partners.
• Experience ensuring SAEs are documented, completed, and reported within protocol-defined timelines.
• Proficiency with Microsoft Office applications.
• Proficiency with EPIC and OnCore™ CTMS is a plus.