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Job Summary: Research Nurse (Study Coordinator) dedicated to coordinating Phase I clinical trials in oncology, ensuring data validity and regulatory compliance for the development of new medications. Key Highlights: 1. Participate in the development of new cancer drugs. 2. Collaborate in cutting-edge clinical trials. 3. Contribute to improving the quality of life of oncology patients. 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 through consultations in global communities, offering them access to cutting-edge clinical trials in the United States and Europe. Currently, with more than 1,300 studies conducted and research centers in the United States, Spain, Portugal, and Ireland, START's mission is to accelerate the development of new cancer drugs that improve patients' quality of life and survival, ultimately leading to their cure. To date, over 43 therapies conducted at START centers have received FDA/EMA approval. Position Available: **Research Nurse \- Study Coordinator** **Responsibilities:** * Identify requirements of Phase I clinical trials, including objectives, cohorts, and patient care needs. * Ensure the validity of data obtained from source documents. * Comply with policies for shipment and handling of biological samples. * Provide all necessary information regarding the clinical trial from its initiation, as well as 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 side effects related to the clinical trial and the investigational drug(s). * Ensure the informed consent process complies with AEMPS, GCP, sponsor, and CEIm regulations. * Collaborate with the Investigator to determine a patient's eligibility for participation in a clinical trial, including documentation of inclusion/exclusion criteria 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 required by 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 change the future of cancer treatment?** Join us in our mission to defeat cancer, trial by trial. Your experience and dedication can help us bring hope and healing to patients worldwide. Submit your application online.
