Early Clinical Innovation Developer

Location:Haifa, IL, 3508504Description:Early Clinical Innovation DeveloperNovocure is a global publicly traded, commercial-stage oncology company developing a profoundly different cancer treatment therapy called tumor treating fields (TTFields) for patients with solid tumors. TTFields therapy is a non-invasive, novel, antimitotic treatment modality that utilizes proprietary technology attempting to slow or reverse tumor progression by inducing tumor cell death.Novocure's commercialized product, Optune, is approved for the treatment of adult patients with glioblastoma (GBM) in the USA, Europe, and Israel.Novocure has ongoing or completed clinical trials and is further expanding its efforts into several other solid tumor indications - non-small cell lung cancer, pancreatic cancer, and other types of solid cancers.The company also conducts innovative studies aiming at improving our technology and expanding the clinical horizons for TTFields Therapy.We are looking for an Early Clinical Study development lead who will provide essential support in the planning, execution, and management of clinical studies in the field of clinical innovation.This role is pivotal in ensuring that our clinical trials are planned, prepared and conducted efficiently, in compliance with regulatory standards, and with the highest level of quality.ESSENTIAL DUTIES AND RESPONSIBILITIES:Plan and develop innovative early-phase clinical studies in collaboration with internal and external experts based on internal data and literature and under the guidance of the head of the departmentPrepare essential clinical study documentsSupport the submission of new studies and amendments to Ethics Committees and Competent AuthoritiesSchedule and coordinate meetings, teleconferences, and site visitsAssist in organizing and distributing study materials and supplies to the investigational site as neededFacilitate communication between internal teams, CRO, and external vendors, ensuring smooth study operationsAbility to build and maintain relationships with various stakeholdersAssist in the preparation of study-related presentations, reports, and summaries for internal and external purposesParticipate in internal and external education regarding such clinical studiesSupport the clinical team in various tasks as needed, contributing to the overall success of the clinical trialsQUALIFICATIONS/KNOWLEDGE:Qualifications:MD or PhD in a related field (medical science, life sciences, healthcare, nursing)CRA/GCP certificate – mustKnowledge:Developing and writing clinical studies protocols- mustPrevious experience in pharma/biotech / medical device company – mustPrevious experience as study coordinator / CRA / MSL – advantageExcellent verbal and written communication skills in English (mother tongue level) – mustProficiency in Microsoft Office (Word, Excel, PowerPoint)OTHER:Strong organizational and time management skills with the ability to handle multiple tasks and prioritize effectivelyExcellent attention to detailGood communication skills in Hebrew and EnglishHigh level of integrity and commitment to maintaining confidentiality and quality standardsAbility to work independently and as part of a collaborative team within a dynamic and fast-paced environmentAdaptability and willingness to learn new skills and take on additional responsibilities as neededA positive attitude and a collaborative approach to problem-solving and teamworkABOUT NOVOCURE:Our visionPatient-forward: aspiring to make a difference in cancer.Our patient-forward missionTogether with our patients, we strive to extend survival in some of the most aggressive forms of cancer by developing and commercializing our innovative therapy.Our patient-forward values– innovation– focus– drive– courage– trust– empathy#IL-GK1