START Center for Cancer Research (“START”) is the world’s largest network of Phase I centers, fully dedicated to oncology clinical research. Throughout our history, START has provided hope to cancer patients in global communities by offering them access to cutting-edge clinical trials in the United States and Europe. Today, with over 1,300 studies conducted and research centers in the United States, Spain, Portugal, and Ireland, START’s mission is to accelerate the development of novel cancer therapies that improve quality of life and survival for cancer patients—and ultimately lead to their cure. To date, more than 43 therapies developed at START centers have received FDA/EMA approval. Available Position: **Research Nurse – Study Coordinator** **Responsibilities:** * Identify requirements of Phase I clinical trials, including objectives, cohorts, and patient care needs. * Ensure validity of data obtained from source documents. * Comply with policies governing shipment and handling of biological samples. * Provide all necessary information regarding the clinical trial—from its initiation onward, including subsequent amendments—to the rest of the research team. * Participate in Initiation Visits. * Complete all required trainings to launch the clinical trial within the Unit. * Educate patients about procedures and adverse effects associated with the clinical trial and the investigational drug(s). * Ensure the informed consent process complies with regulations set forth by the Spanish Agency for Medicines and Health Products (AEMPS), Good Clinical Practice (GCP), the sponsor, and the Independent Ethics Committee (CEIm). * Collaborate with the Principal Investigator to determine a patient’s eligibility for participation in a clinical trial, including documentation of inclusion/exclusion criteria as specified in the protocol. * Guarantee adherence to the protocol schedule for events and requirements (queries). * Conduct follow-up/safety/survival calls to patients per protocol after the patient completes trial treatment, for the duration specified in the protocol. **Requirements:** * Nursing degree. * Interest in the healthcare field. * Proactive individual with strong organizational skills. * Excellent sense of responsibility and attention to detail. * Ability to work collaboratively and maintain effective communication with colleagues and supervisors. * Intermediate level of English. **Are you ready to join a team that will transform the future of cancer treatment?** Join us in our mission to defeat cancer—one clinical trial at a time. Your experience and dedication can help bring hope and healing to patients worldwide. Submit your application online.