Clinical Research Associate
Allucent
Posted: 10/21/2026
Clinical Research Associate I – Clinical Research Associate II
Precision For Medicine
Posted: 10/15/2026
Clinical Research Associate I/II
Precision Medicine Group
Posted: 10/15/2026
Clinical Scientist – Oncology
Excelya
Posted: 10/15/2026
Clinical Research Associate
Novo Nordisk
Posted: 10/14/2026
Clinical Research Associate (CRA) Monitor – Consultant
Ividata Life Sciences
Posted: 10/7/2026
Senior Biostatistician – Biomarker Experience
ICON plc
Posted: 10/6/2026Biostatistician – Biomarker Experience
ICON plc
Posted: 10/6/2026Senior Clinical Research Associate – Contractor
Allucent
Posted: 10/3/2026Clinical Research Associate – Investigator Site
Excelya
Posted: 9/25/2026
Clinical Research Manager – Local Trial Manager
Parexel
Posted: 9/24/2026Clinical Scientist – Immunology
Excelya
Posted: 9/23/2026Senior Clinical Research Associate
Precision For Medicine
Posted: 9/21/2026Senior Clinical Research Associate
Precision For Medicine
Posted: 9/21/2026Senior Clinical Research Associate
Precision For Medicine
Posted: 9/21/2026Senior Clinical Research Associate
Precision For Medicine
Posted: 9/21/2026Senior Clinical Research Associate
Precision Medicine Group
Posted: 9/21/2026Senior Clinical Research Associate
Precision Medicine Group
Posted: 9/21/2026Senior Clinical Research Associate
Precision Medicine Group
Posted: 9/21/2026Senior Clinical Research Associate
Precision Medicine Group
Posted: 9/21/2026Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in managing clinical trial monitoring activities, ensuring compliance with ICH-GCP and regulatory guidelines while fostering strong site relationships. Proficient in both English and French, with a focus on independent work and effective communication.
Highest-signal resume keywords
Clinical Trial MonitoringICH-GCP ComplianceRegulatory AffairsBilingual CommunicationSite Relationship Management
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 start-up
- Travel throughout France
Requirements
What you’ll need- Experience in leading monitoring activities in complex trials with a minimum of 2 years’ experience
- Strong understanding of ICH-GCP and regulatory guidelines
- Clear and confident communicator in English and French
- Comfortable working independently and managing priorities
- Willingness to travel, as required (8 DOS per month)
Benefits
Comp & perks- Comprehensive benefits package per location
- Competitive salaries per location
- Departmental Study/Training Budget for furthering professional development
- Flexible Working hours (within reason)
- Participation in our enriching Buddy Program as a new or existing employee
- Internal growth opportunities and career progression
- Financially rewarding internal employee referral program
- Eligibility for our Spot Bonus Award Program in recognition of going above and beyond on projects
- Eligibility for our Loyalty Award Program in recognition of loyalty and commitment of longstanding employees
- Prescribing 2 days in office per week for employees within reasonable distance from one of our global offices
ATS Keywords
✓ Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Clinical Trial ManagementMonitoring ActivitiesRegulatory ComplianceData CollectionSite Activation
Soft Skills
Independent WorkProblem SolvingCommunication
Industry Keywords
GCPICHSOPsPatient SafetyTrial Integrity