Senior Clinical Research Associate & Lead task

Resourcing Group; Netherlands; On-site; EUR 65,000 - 75,000; Full time

Benefits offered by this job

Company car

Job summary

Resourcing Group represents a Global CRO seeking a Clinical Research Associate (CRA) to coordinate CRAs in Europe and lead experienced teams. The role focuses on monitoring trials in phases II-III, ensuring GCP compliance, and site initiation/close-out across sites.

FTE 1.0 with a salary of 65–75k EUR plus a company car. The ideal candidate will hold a life-sciences degree and have 2+ years CRA monitoring experience in CRO/Pharma/Biotech settings, including commercial studies, with strong

Qualifications

• Bachelor degree in life-science.
• Min 2 year monitoring experience as CRA within a CRO, Pharma, Biotech in Belgium.
• Experience in commercial studies.
• Experience with site initiation, site close out.
• Experience in clinical studies phase II-III.
• FTE: 1.0.
• Salary between 65000 - 75000 euro gross plus company car.

Responsibilities

• Coordinate other CRAs in Europe for one of your studies.
• Provide leadership tasks for experienced CRAs with over 3 years of experience.
• Monitor clinical studies in phases II-III.
• Ensure adherence to GCP, investigator integrity, and all study procedures.
• Identify, qualify and initiate investigators and their sites.
• Supervise study conduct according to GCP and applicable laws.

Skills

Monitoring experience

Leadership

GCP knowledge

Education

Bachelor's degree in life-science

Job description

Our client is a Global CRO currently supporting various Pharmaceutical & Biotech companies globally. They offer a full service solution encompassing clinical & non-clinical development, peri-approval & market access. They are currently seeking a CRA / Clinical Research Associate

Job Overview

• Opportunity to coordinate other CRAs in Europe for one of your studies.
• Leadership tasks for experienced CRAs with over 3 years of experience
• Monitoring clinical studies in phases II-III
• Assuring adherence to Good Clinical Practices, investigator integrity, and compliance with all study procedures.
• Identification, qualification and initiation of investigators and their sites.
• Supervising study conduct according to GCP requirements and all applicable laws.

Key Requirements

• Bachelor degree in life-science
• Min 2 year monitoring experience as CRA within a CRO, Pharma, Biotech in Belgium
• Experience in commercial studies
• Experience with site initiation, site close out
• Experience in clinical studies phase II-III
• FTE: 1.0
• Salary between 65000 - 75000 euro gross plus company car