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.

We are looking for a CRA who will provide essential support in the planning, execution, and management of clinical trials.

This role is pivotal in ensuring that our clinical trials are conducted efficiently, in compliance with regulatory standards, and with the highest level of quality.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

• Assist in the preparation of essential clinical trial documents
• Schedule and coordinate meetings, teleconferences, and site visits
• Assist in organizing and distributing study materials and supplies to the investigational site
• 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
• Support the clinical team in various tasks as needed, contributing to the overall success of the clinical trials

QUALIFICATIONS/KNOWLEDGE:

Qualifications:

• Bachelor’s degree in related field (medical science, life sciences, healthcare, nursing) – must
• Master’s degree in related field – advantage
• CRA/GCP certificate – must

Knowledge

• At least 2 years of  experience as study coordinator / CRA – must
• Previous experience in pharma/biotech/medical device – advantage

OTHER:

• 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