Early Clinical Innovation Developer

Novocure 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 department
• Prepare essential clinical study documents
• Support the submission of new studies and amendments to Ethics Committees and Competent Authorities
• Schedule and coordinate meetings, teleconferences, and site visits
• Assist in organizing and distributing study materials and supplies to the investigational site as needed
• Facilitate communication between internal teams, CRO, and external vendors, ensuring smooth study operations
• Ability to build and maintain relationships with various stakeholders
• Assist in the preparation of study-related presentations, reports, and summaries for internal and external purposes
• Participate in internal and external education regarding such clinical studies
• Support the clinical team in various tasks as needed, contributing to the overall success of the clinical trials
  
  

• Qualifications:
• MD or PhD in a related field (medical science, life sciences, healthcare, nursing)
• CRA/GCP certificate – must
• Knowledge:
• Developing and writing clinical studies protocols- must
• Previous experience in pharma/biotech / medical device company – must
• Previous experience as study coordinator / CRA / MSL – advantage
• Excellent verbal and written communication skills in English (mother tongue level) – must
• Proficiency in Microsoft Office (Word, Excel, PowerPoint)
  
  

• Strong organizational and time management skills with the ability to handle multiple tasks and prioritize effectively
• Excellent attention to detail
• Good communication skills in Hebrew and English
• High level of integrity and commitment to maintaining confidentiality and quality standards
• Ability to work independently and as part of a collaborative team within a dynamic and fast-paced environment
• Adaptability and willingness to learn new skills and take on additional responsibilities as needed
• A positive attitude and a collaborative approach to problem-solving and teamwork