Responsibilities:

• Oversee all aspects of clinical trial development and execution.
• Design clinical trial protocols based on research and study objectives.
• Develop and manage study timelines, metrics, and data review plans.
• Lead clinical study teams, including CROs, CRAs, and site personnel.
• Ensure compliance with GCP guidelines, regulations, and SOPs.
• Develop and maintain clinical study documentation.
• Coordinate regulatory submissions and interactions with review boards.
• Manage clinical study budget and resources.

Qualifications:

• Minimum 5 years clinical trial experience, including 2+ years in trial management.
• Strong project management, communication, and interpersonal skills.
• In-depth knowledge of GCP, ICH, and regulatory requirements.
• Experience in clinical study design, data analysis, and reporting.
• Ability to lead and mentor clinical research teams.
• Bachelor’s degree in science or related field; advanced degree preferred.

Preferred:

• Experience in psychiatric disorders research.
• Statistical design knowledge.
• Clinical trial certification.

Note: Hebrew and English fluency required; additional language skills beneficial.