Responsibilities:

• Lead and manage clinical development plans, including pre-clinical and clinical studies.
• Collaborate with stakeholders to define and design pre-clinical and clinical studies meeting development goals and regulatory requirements.
• Oversee all aspects of clinical research, potentially including Quality Assurance (QA).
• Manage interactions with regulatory agencies (e.g., Israeli MOH) and contract research organizations (CROs).
• Prepare and manage clinical documentation.

Qualifications:

• Minimum 10 years of experience conducting clinical studies.
• Design and define clinical and pre-clinical studies based on development needs and regulatory requirements.
• Experience working with the Israeli Ministry of Health (MOH) and contract research organizations (CROs).
• Expertise in preparing clinical documentation.
• Strong team leadership skills and a collaborative work style.