Raz Ben-Haim

• Managed cross-functional project teams to deliver projects on time and within budget
• Led project planning and execution, including budget management and resource allocation
• Identified and mitigated project risks to proactively reduce potential issues
• Facilitated meetings, conducted presentations, and reported on project performance metrics
• Communicated project status updates and issues to key stakeholders regularly
• Managed cross-functional teams to implement site activation plans and meet project objectives
• Successfully led the activation of multiple sites, ensuring timely completion and project success
• Coordinated with vendors and contractors to oversee site deployment and installation processes
• Developed and maintained relationships with key stakeholders to drive site activation efforts
• Performed site surveys and assessments to identify potential challenges and develop mitigation strategies
• Complete submissions and notifications to regulatory authorities, ethics committee and other bodies
• Performs recruitment of study sites
• Supporting site contracts negotiations
• Assisted in the development and implementation of clinical trial procedures and documentation
• Communicated with study sites, sponsors, and regulatory authorities to ensure compliance with study protocols
• Contributed to the preparation and submission of regulatory documents and study reports
• Ensured data quality and integrity by conducting regular source data verification and monitoring activities

• Handled emergency cases and critical care at different veterinary centers.
• Managed day-to-day operations and inventory
• Provided preventive care and vaccinations to a variety of animals
• Educated pet owners on proper treatment and wellness for their animals
• Managed complex conditions in a wide variety of therapeutic areas in Internal Medicine
• Improved patient outcomes by accurately diagnosing and treating various animal illnesses and injuries.

• Managed cross-functional teams to implement site activation plans and meet project objectives.
• Successfully led the activation of multiple sites, ensuring timely completion and project success.
• Coordinated with vendors and contractors to oversee site deployment and installation processes.

• Developed and maintained relationships with key stakeholders to drive site activation efforts.
• Performed site surveys and assessments to identify potential challenges and develop mitigation strategies. · Complete submissions and noti cations to regulatory authorities, ethics committee and other bodies.
• Performs recruitment of study sites
• Supporting site contracts negotiations

Assisted in the development and implementation of clinical trial procedures
and documentation.

Communicated with study sites, sponsors, and regulatory authorities to ensure
compliance with study protocols.

Contributed to the preparation and submission of regulatory documents and
study reports.

Ensured data quality and integrity by conducting regular source data
verification and monitoring activities