Job Description

Overview Join to apply for the Clinical Research Coordinator role at The START Center for Cancer Research . The START Center for Cancer Research ("START") is the world’s largest early phase site network, fully dedicated to oncology clinical research. START’s mission is to accelerate the development of new anticancer drugs to improve quality of life and survival for patients with cancer. START supports access to cutting-edge trials through its eight clinical trial sites in the United States and Europe. START represents the world’s largest roster of Principal Investigators (PIs) across its sites and is committed to accelerating passage from trials to treatments. We are hiring a motivated Clinical Research Coordinator (CRC) who 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. This role involves direct patient interaction, data collection, and maintaining compliance with Good Clinical Practice (GCP). The CRC will be assigned multiple protocols and will oversee planning and coordinating patient participation, as well as implementing protocol-specific requirements and providing up-to-date information to the team. Responsibilities Communicate regularly with Study Sponsors, CROs, staff, and others regarding protocol questions, concerns, and status. Monitor the day-to-day conduct of assigned studies in accordance with protocols, SOPs, and GCP to ensure study integrity. Create or review forms to assure protocol compliance; maintain study files with standardized labeling procedures. Implement initial protocol and amendments; train staff involved in patient treatment and management. Maintain an up-to-date contact list and assist with patient screening and eligibility determinations. Facilitate the informed consent process and ensure consent is appropriately completed. Prepare and manage source documents according to SOPs. Identify deviations to the protocol and work with leadership to address corrective actions. Assist the data coordination 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 activities in conjunction with the data coordinator. Provide documentation for all deviations related to the protocol or SOPs and ensure understanding across the team. Required Education And 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 & Travel Requirements Approximately 80% of time is spent sitting. Fast-paced and changing healthcare environment with demanding deadlines. Constant need for updating knowledge; works closely with physicians and ancillary personnel in caring for oncology/hematology patients. Benefits Competitive compensation based on experience. Comprehensive health coverage: Medical, dental, and vision insurance. Robust retirement planning: 401(k) with employer matching. Life and disability insurance; health savings and flexible spending accounts. Paid time off, flexible schedule, remote work options where applicable. A collaborative, creative environment that supports learning and growth. More About The START Center For Cancer Research Deeply rooted in community oncology centers globally, START provides access to specialized preclinical and early-phase clinical trials of novel anti-cancer agents. START clinical trial sites have conducted many early-phase trials and supported therapies that were FDA-approved. Learn more at STARTresearch.com. Ready to be part of a team changing the future of cancer treatment? Submit your application online. We are an equal opportunity employer that values diversity and does not discriminate based on race, color, religion, marital status, age, national origin, ancestry, disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected by law. #J-18808-Ljbffr The START Center for Cancer Research

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