Experienced Clinical Research Associate- Oncology- Israel
Core
Conduct site qualification, initiation, monitoring, and close-out visits for oncology clinical trials to ensure patient safety, data integrity, and protocol compliance.
Role type
Senior Clinical Research Associate (Oncology)
Builds
Clinical trial execution and site management for pharmaceutical/biotech sponsors
Domain
Life Sciences / Clinical Research / Oncology
Deliverable
client delivery
Required skills
GCP/ICH guidelines knowledge, site monitoring, patient recruitment strategies, risk assessment, regulatory documentation management, cross-functional collaboration
Preferred skills
Sponsor-dedicated or cFSP environment experience, study start-up knowledge
Technologies
Trial Master Files (TMF), Investigator Site Files (ISF)
Responsibilities
Conduct site qualification, initiation, monitoring, and close-out visits; Ensure investigational sites maintain high standards of patient safety and data integrity; Build and maintain effective relationships with investigators; Monitor study progress and resolve data queries; Collaborate on patient recruitment and retention strategies; Maintain accurate study documentation; Identify and escalate study risks; Mentor junior clinical team members
Seniority
Mid-Senior, hands-on IC
