In-House Clinical Research Coordinator: Trials & Data Lead

U.S. Urology Partners; Île-de-France; Hybrid; EUR 30,000 - 59,000; Full time

Benefits offered by this job

Medical plans

Dental plans

Vision plans

HSA / FSA

401(k) matching

Employee Assistance Program (EAP)

Job summary

U.S. Urology Partners is seeking an In-House Clinical Research Coordinator to conduct and document clinical trials in accordance with Good Clinical Practice guidelines. The role requires coordinating a team, recruiting subjects, obtaining informed consent, and ensuring regulatory compliance.

Responsibilities include data handling, adverse event reporting, and collaboration with sponsors to support protocol addenda and audits.

Qualifications

• Bachelor's or Associate degree required.
• GCP Certification required.
• IATA Certificate required.
• CCRC certification (ACRP/SoCRA) required.
• 2–3 years related research experience preferred.

Responsibilities

• Coordinate a team to conduct a minimum of six clinical trials and evaluate/analyze data.
• Recruit study subjects based on protocol criteria.
• Discuss protocols with patients and obtain informed consent.
• Ensure accuracy of source documentation and CRFs per FDA guidelines.
• Report adverse events per study protocol and monitor safety.
• Prepare for sponsor meetings and ensure protocol understanding.

Skills

GCP Certificate

IATA Certificate

CCRC Certification

Clinical Research

Education

Associates or Bachelor's Degree

Job description

U.S. Urology Partners is seeking an In-House Clinical Research Coordinator to conduct and document clinical trials in accordance with Good Clinical Practice guidelines. The role requires coordinating a team, recruiting subjects, obtaining informed consent, and ensuring regulatory compliance.

Responsibilities include data handling, adverse event reporting, and collaboration with sponsors to support protocol addenda and audits.