Apply

Ready to go for it?

AI Apply speeds things up—apply directly if you prefer.

FREE ACCESS
5,000–10,000 jobs/day
Scoutfield Logo

See all jobs on Scoutfield

Search thousands of fresh jobs every day.

Discover
  • Fresh listings
  • Fast filters
  • No subscription required
Create a free account and start exploring right away.
Allucent

Senior Clinical Research Associate – Contractor

Allucent

. Independently manage all aspects of monitoring for assigned clinical trials across study phases, including site initiation, routine monitoring, and close-out visits .

Posted 10/3/2026part-timeParis • FranceSeniorWebsite

Core Competencies

Role fit
Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates extensive experience in managing clinical trial monitoring activities, ensuring compliance with ICH-GCP and regulatory guidelines while maintaining strong relationships with sites. Proficient in both English and Hebrew, with a focus on high-quality data collection and trial integrity.

Highest-signal resume keywords
Clinical Trial MonitoringICH-GCP ComplianceRegulatory AffairsSite Relationship ManagementBilingual Communication

ATS Keywords

Tailor your resume
Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills
Clinical Trial ManagementRegulatory ComplianceData CollectionSite ActivationMonitoring Activities
Soft Skills
Independent WorkProblem SolvingCommunication
Industry Keywords
Oncology TrialsRare Disease TrialsSOPsPatient SafetyStudy Startup

About the role

Key responsibilities & impact
  • Independently manage all aspects of monitoring for assigned clinical trials across study phases, including site initiation, routine monitoring, and close-out visits
  • Ensure compliance with protocols, GCP, ICH, SOPs, and applicable regulatory requirements
  • Build strong site relationships, acting as a primary point of contact and ensuring high-quality data collection
  • Identify and resolve site issues, escalating as needed to maintain trial integrity and patient safety
  • Perform activities around regulatory affairs, site activation, and study startup
  • Own investigator-site relationships and serve as a bridge between sponsor and site
  • Travel throughout Israel

Requirements

What you’ll need
  • Minimum of at least 5 years’ experience leading monitoring activities in complex trials, ideally in oncology or rare disease
  • Strong understanding of ICH-GCP and regulatory guidelines
  • Clear and confident communication in English and Hebrew
  • Comfortable working independently and managing priorities
  • Willingness to travel, as required