Experienced Clinical Research Associate - Oncology

About the role

iQVIA's Clinical Functional Service Partnership (CFSP) offers an experienced Clinical Research Associate position in oncology, based in Netanya, Israel. The role involves monitoring clinical trials at sites, building relationships with investigators and supporting study quality, within a partnership model that combines specialist program depth with the global infrastructure of iQVIA.

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.