Freelance Senior Clinical Research Associate (DU/EN + FR)

Oxford Global Resources; Vlaams-Brabant; Sur place; EUR 61 000 - 95 000; Plein temps

Résumé du poste

Oxford Global Resources is seeking an experienced Senior CRA for a freelance, full-time project starting asap in Belgium. You will monitor clinical sites, manage timelines, and ensure data quality while working remotely with on-site visits.

You will lead onsite monitoring, perform CRF reviews, and cooperate with vendors, investigators and internal teams; fluency in Dutch and English and French is required; travel is expected.

Qualifications

• BSc or MSc in Life Sciences (or equivalent)
• Independent on-site monitoring experience in Belgium, ideally on multiple projects
• Experience in Phase II/III monitoring visits
• Experience supporting Oncology/Hematology and Infectious disease studies
• Fluency in Dutch and English, with professional proficiency in French
• Full and clean driver's license and willingness to travel
• Intermediate to advanced knowledge of MS Office

Responsabilités

• Conduct onsite monitoring visits and reporting
• Perform CRF reviews, source data verification and query resolution
• Be responsible for site communication and management
• Supervise study activities, timelines, and site schedules
• Act as a point of contact for in-house support services and vendors
• Support quality control, such as compliance monitoring and reports review

Connaissances

On-site monitoring

Study coordination

Stakeholder communication

Quality compliance

MS Office

Travel readiness

Formation

BSc/MSc in Life Sciences

Outils

MS Office

Description du poste

Are you an experienced freelance CRA and have full-time availability for a project to start asap? You will be welcomed in a global company in which team spirit is key.

Job Description

As a Senior CRA, you will work on the frontline of communication with project stakeholders, ensuring timelines, targets and standards of clinical research projects in a variety of therapeutic indications. You will build and maintain relationships with clinical sites and investigators. Your focus will be on subjects' rights, safety and well-being and quality of data compliance.

Responsibilities

• Conducting and reporting all types of onsite monitoring visits
• Performing CRF reviews, source document verification and query resolution
• Be responsible for site communication and management
• Supervising study activities, timelines, and schedules for each site
• Acting as a point of contact for in-house support services and vendors
• Supporting quality control, such as compliance monitoring and reports review

Requirements

• BSc or MSc in Life Sciences (or similar), or an equivalent combination of education, training & experience
• Independent on-site monitoring experience in Belgium, ideally on multiple projects at a time
• Demonstrable experience in all types of monitoring visits in Phase II and/or III
• Experience supporting Oncology/ Hematology and Infectious disease studies
• Fluency in Dutch and English, with professional proficiency in French
• Full and clean driver's license, and the ability to travel
• Intermediate to Advanced knowledge of MS Office.

Contract Information

• Freelance opportunity
• Full-time (80% is not an option)
• Fully remote work + on-site visits
• 6 months contract
• Start-date : October the latest