Experienced Clinical Research Associate (Clinical Research)

Location: Netanya, Israel

Company

hirify.global provides clinical research services, commercial insights, and healthcare intelligence for the life sciences and healthcare industries.

What you will do

• Conduct site selection, initiation, monitoring, and close-out visits according to the study scope, protocol, GCP, ICH guidelines, and regulatory requirements.
• Support site subject recruitment plans, track enrollment, and help improve recruitment predictability.
• Deliver protocol and study-related training while maintaining regular communication with assigned sites.
• Evaluate site quality and protocol compliance, escalate issues, and create monitoring reports, follow-up letters, and action plans.
• Track regulatory submissions, approvals, CRF completion, data queries, and resolutions; support study start-up when required.
• Maintain TMF and ISF documentation and support site financial management and invoice retrieval where applicable.

Requirements

• At least 2 years of on-site monitoring experience.
• High school diploma or equivalent; a degree in a scientific or healthcare discipline is preferred.
• Knowledge of clinical research regulations, including GCP and ICH guidelines.
• Therapeutic and protocol knowledge acquired through company training.
• Proficiency with Microsoft Word, Excel, PowerPoint, laptops, and applicable mobile devices.
• Good written and verbal English communication skills are required.

Culture & Benefits

• Collaborate with study team members, sites, clients, managers, and coworkers to support project execution.
• Apply organizational, problem-solving, time-management, and financial-management skills across assigned studies.
• Work within a global clinical research and healthcare intelligence organization.