Hybrid CRA: Site Monitoring & Start-Up Expert

CTI Clinical Trial and Consulting Services; France; On-site; EUR 55,000 - 75,000; Full time

Job summary

CTI Clinical Trial and Consulting Services seeks a Clinical Research Associate to oversee monitoring activities at assigned study sites in Germany. You will ensure quality deliverables and regulatory compliance while coordinating with cross‑functional teams.

The role involves site visits (PSV, SIV, IMV, COV), regulatory documentation, and ongoing collaboration with project teams. 3‑5 years CRA experience and fluent English are required.

Qualifications

• 3 - 5 years clinical research experience as a CRA or related profession in Germany, incl. independent monitoring.
• Life science background.
• Fluent English (B2) in speech and writing.

Responsibilities

• Serve as main CTI contact for assigned study sites.
• Conduct site visits and complete deliverables per Monitoring Plan.
• Assist with startup activities and site selection.
• Collect, review and track essential regulatory documents.
• Monitor site status and report to the Clinical Project Manager.

Skills

CRA experience

Independent monitoring

ICH-GCP knowledge

English proficiency

Life science background

Job description

CTI Clinical Trial and Consulting Services seeks a Clinical Research Associate to oversee monitoring activities at assigned study sites in Germany. You will ensure quality deliverables and regulatory compliance while coordinating with cross‑functional teams.

The role involves site visits (PSV, SIV, IMV, COV), regulatory documentation, and ongoing collaboration with project teams. 3‑5 years CRA experience and fluent English are required.