Clinical Research Associate 2 - Israel

About the role

iQVIA's Clinical Functional Service Partnership (CFSP) offers embedded clinical research associates the variety and sponsor-level exposure of working within a leading pharmaceutical or biotechnology team, backed by IQVIA's global infrastructure and career support. This Clinical Research Associate 2 position in Israel involves site monitoring and building relationships with investigators across studies in various therapeutic areas.

Key responsibilities

• Conduct site qualification, initiation, monitoring and close-out visits according to study protocols, GCP, ICH guidelines and regulatory requirements.
• Ensure sites maintain high standards of patient safety, data integrity, protocol compliance and study quality.
• Build and maintain relationships with investigators and site personnel, providing guidance, training and support.
• Monitor study progress, including regulatory documentation, patient recruitment and enrollment, data query resolution and site performance metrics.
• Help sites implement and optimise patient recruitment and retention strategies.
• Maintain accurate, inspection-ready documentation such as Investigator Site Files, Trial Master Files, monitoring reports and follow-up communications.
• Identify and escalate study risks, site issues and quality concerns, and mentor junior team members through coaching, training and co-monitoring.

Required profile

• University degree in Life Sciences, Health Sciences, Nursing, Pharmacy or a related discipline, or equivalent education and experience.
• At least 2 years of on-site monitoring experience of clinical trials within a CRO, pharmaceutical, biotechnology or healthcare environment.
• Fluent written and spoken Hebrew (minimum C1 level) and a strong command of English.
• Willingness to travel within the assigned region (up to 40-60% of working time) and a valid Class B driver's licence.

Required skills

• Strong knowledge of GCP, ICH guidelines and applicable regulatory requirements.
• Preferrable: experience in a sponsor-dedicated or CFSP environment, and knowledge of patient recruitment and study start-up.
• Excellent communication, organisational and stakeholder management skills.