Clinical Research Coordinator

Clinical Research Coordinator We are hiring a Clinical Research Coordinator to work under the guidance of senior research staff to support the daily activities of early phase oncology clinical trials. The CRC ensures the accurate and timely conduct of clinical research, adhering to protocols, regulatory requirements, and patient safety standards. Pay range: $30.00 to $44.00 per hour, based on experience, qualifications, and internal equity. Employees in this role may be eligible for an annual bonus of up to 10% of base earnings. Work schedule: 8:00 am-5:00 pm EST, Monday-Friday. Location: 405 Lakeville Road, Entrance A, Lake Success, NY 11042. Essential Responsibilities Communicate regularly with study sponsor, CRO, and staff regarding questions, concerns, and protocol status. Monitor day‑to‑day conduct of assigned studies according to protocol, SOP, and Good Clinical Practice to ensure study integrity. Create and review study documents to assure protocol compliance. Maintain files using standardized study document labeling and filing procedures. Implement initial protocol and amendments and train staff involved in patient treatment and management. Maintain an up‑to‑date contact list. Assist with patient screening and eligibility determination. Facilitate the informed consent process ensuring that consent is appropriately completed. Prepare and manage source documents according to standard operating procedures. Recognize protocol deviations and work with leadership and staff to address corrective actions. Assist data coordinator team with case report form completion and query resolution. Work with the Principal Investigator to complete and submit Serious Adverse Event reports. Perform protocol‑specific closeout related activities in conjunction with the data coordinator. Provide documentation for all deviations, whether related to the protocol or an SOP. Ensure all team members understand and adhere to assigned protocols. Education & Experience High School Diploma or GED. 2 years of clinical research experience. Basic understanding of oncology clinical trials, particularly Phase 1 studies. Strong attention to detail and accuracy in data collection and documentation. Ability to manage multiple tasks and meet deadlines in a fast‑paced environment. Excellent organizational and time‑management skills. Strong communication skills, both written and verbal. Ability to interact professionally with patients, study staff, and external stakeholders. Working knowledge of GCP and regulatory requirements. Proficient in Microsoft Office Suite and clinical trial management software. Preferred Education and Experience Experience working in an oncology setting. Physical and Travel Requirements Approximately 80% of time spent sitting. Fast‑paced and ever‑changing healthcare environment. Demanding deadlines and time frames. Constant demand for updating knowledge. Works closely with physicians and ancillary personnel caring for oncology/hematology patients. Benefits and Perks 401(k) retirement savings plan with employer match. Eligibility for an annual performance bonus based on role and company results. Generous paid time off and paid holidays. Comprehensive medical, dental, and vision coverage and optional insurance options. Company‑paid life and disability insurance for additional financial protection. Employee Assistance Program (EAP) providing confidential, no‑cost support for employees and families from day one. Flexible FSA and HSA plans to support financial wellness. Commitment to a supportive environment that values balance, well‑being, and flexibility. We are an equal opportunity employer that welcomes and encourages diversity in the workplace. We do not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law. #J-18808-Ljbffr START Research