Senior Clinical Research Associate – Oncology (Israel)

About the role

ICON plc is seeking an experienced Senior Clinical Research Associate (CRA) to support oncology clinical trials in Israel. The role involves overseeing trial sites, ensuring compliance with protocols, and safeguarding participant safety while contributing to high‑quality data collection.

Key responsibilities

• Monitor clinical trial sites to verify adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.
• Conduct site visits, assess performance, resolve issues, and provide on‑site support.
• Collaborate with cross‑functional teams to ensure timely, accurate data collection and reporting.
• Provide training and guidance to site staff and junior CRAs to maintain high standards of trial conduct.
• Build and maintain effective relationships with site personnel and stakeholders to facilitate smooth trial operations.

Required profile

• Advanced degree in life sciences, nursing, medicine, or a related field.
• At least 3 years of experience as a Clinical Research Associate, preferably with oncology trials and sponsor‑dedicated projects.
• Demonstrated ability to manage multiple sites and projects simultaneously.
• Strong organizational, problem‑solving, and stakeholder‑management skills.
• Fluent written and verbal communication in Hebrew and English.
• Willingness to travel up to 60% of the time and a valid driver’s license.

Required skills

• Proficiency with clinical trial monitoring practices and data integrity processes.
• Experience using clinical trial software and tools.

What we offer

• Competitive salary and benefits package tailored to the local market.
• Health insurance options for you and your family.
• Generous annual leave entitlements.
• Retirement planning programs.
• Supportive, inclusive culture that encourages professional growth.