Clinical Research Coordinator II - Tisch Cancer Center

Job Description A Clinical Research Coordinator (CRC) II position is currently available within the Tisch Cancer Center. Duties will include data collection and management of patient clinical information, timely collection of protocol related samples including shipment to outside entities as required, obtain informed consent, collect, maintain and organize study information, and assist with other day‑to‑day operations as required. Under minimal supervision, the Clinical Research Coordinator II will manage a workload that includes studies of increased complexity. Responsibilities Coordinate activities of ongoing clinical trials including answering phone calls, screening participants for eligibility, registering subjects with sponsoring agency, and administering lifestyle questionnaires. Obtain informed consent under supervision of the study investigator(s) and educate participants regarding study requirements. Screen patients for eligibility and register subjects with sponsoring agency. Coordinate research team to ensure compliance with planned treatment protocol, including required laboratory and radiographic testing. Secure, deliver, and ship blood and/or tissue samples, radiographs, and other clinical specimens as required by protocol. Act as liaison between investigators and sponsoring agency. Coordinate activities pertinent to safeguarding patients’ rights in research. Ensure accurate and complete compilation of subject data through chart reviews. Collect and record study data on Case Report Forms (CRFs) and submit forms in a timely manner according to study guidelines. Meet with internal and sponsor‑appointed monitors to ensure accuracy of subject data and compliance with research protocol. Maintain source documents and subject files in accordance with Mount Sinai School of Medicine (MSSM) Standard Operating Procedures (SOPs). Assist with analyzing data as needed. Report adverse events and serious adverse events in accordance with MSSM Institutional Review Board (IRB) SOPs, sponsor guidelines, and federal regulations. Assist the PI and regulatory staff in the preparation of new protocol submissions, protocol amendments, and renewals of ongoing clinical trials. Participate in investigators’ meetings and assist with coordinating study initiation visits. Attend divisional/departmental/institutional educational and training seminars. Contact local physicians to obtain source documentation and subject survival status. Educate new staff regarding the overview of clinical research, office policy and procedures, data submission, patient registration, and specimen handling. Qualifications Bachelor's degree in sciences or related field. 2 years of clinical research experience. Oncology experience preferred. Equal Opportunity Employer The Mount Sinai Health System is an equal opportunity employer, complying with all applicable federal civil rights laws. We do not discriminate, exclude, or treat individuals differently based on race, color, national origin, age, religion, disability, sex, sexual orientation, gender, veteran status, or any other characteristic protected by law. We are deeply committed to fostering an environment where all faculty, staff, students, trainees, patients, visitors, and the communities we serve feel respected and supported. Compensation The salary range for the role is $66,199.99 - $90,000.04 annually. Actual salaries depend on a variety of factors, including experience, education, and operational need. The salary range or contractual rate listed does not include bonuses/incentive, differential pay or other forms of compensation or benefits. #J-18808-Ljbffr Mount Sinai Morningside