Early Clinical Innovation Lead

1 week ago

Haifa, Haifa, Israel Novocure Full time $104,000 - $130,878 per year

We are looking for a 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.

Full-time role combining office work at our R&D Center in Haifa with field work, including hospital visits and collaboration with professional teams.

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.
  • Support the clinical team in various tasks as needed, contributing to the overall success of the clinical trials.

QUALIFICATIONS/KNOWLEDGE:

  • Qualifications:
  • MD, PhD, or MSc with thesis in a related field (medical science, life sciences, healthcare, nursing).

  • CRA/GCP certificate – must.

  • Knowledge:

  • Excellent verbal and written communication skills in English (mother tongue-level) – must.
  • Previous experience in pharma/biotech / medical device company – must.
  • Previous experience as a study coordinator / CRA – advantage.
  • Proficiency in Microsoft Office (Word, Excel, PowerPoint).

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 and additional responsibilities as needed.
  • A positive attitude and a collaborative approach to problem-solving and teamwork.

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