Clinical Research Coordinator

We are currently hiring a Clinical Research Coordinator. The Clinical Research Coordinator (CRC) will 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. Work Schedule: Monday‑Friday 8:00 am‑5:00 pm Location: START – East Brunswick, NJ The annual base salary for this role is $55/hour–$60/hour. Base pay may vary depending on location, experience, education, and other factors. Essential Responsibilities Communicate regularly with Study Sponsor’s, CRO’s, staff, and others regarding questions, concerns, and protocol status. Monitor daily conduct of assigned studies to ensure compliance with protocol, SOPs, and GCP. Create and review forms for assigned trials to assure protocol compliance. Maintain study documents using standardized labeling and filing procedures. Implement protocol initial and amendments, training staff involved in patient treatment. Maintain an up‑to‑date contact list. Assist with patient screening and determination of eligibility. Facilitate the informed consent process. Prepare and manage source documents per SOP. Recognize protocol deviations and work with leadership 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 close‑out activities with the data coordinator. Provide documentation for all deviations related to protocol or SOP. Ensure team members understand and adhere to assigned protocols. Required Education and Experience High School Diploma or GED. Minimum 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 written and verbal communication skills. Professional interaction with patients, study staff, and external stakeholders. Knowledge of GCP and regulatory requirements. Proficiency in Microsoft Office Suite and clinical trial management software. Preferred Education and Experience Experience working in an oncology setting. Benefits and Perks 401(k) retirement savings plan with employer match. Eligibility for an annual performance bonus. Generous paid time off and paid holidays. Comprehensive medical, dental, and vision coverage and optional insurance options. Company‑paid life and disability insurance. Employee Assistance Program (EAP) providing confidential support. Flexible FSA and HSA plans. 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 The START Center for Cancer Research