Freelance Senior Clinical Research Associate

SmartRecruiters, Inc.; Brussel; Sur place; EUR 83 000 - 124 000; Plein temps

Résumé du poste

PSI CRO is seeking a Freelance Senior Clinical Research Associate in Belgium to lead on-site monitoring, ensure data quality and compliance, and maintain timely study milestones.

You will manage site communications, perform source data verification, support vendors, and coordinate monitoring visits across Phase II/III oncology, hematology, and infectious disease studies.

Fluent in Dutch and English with French proficiency, a valid driver’s license, and willingness to travel are required.

Qualifications

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

Responsabilités

• Conducting and reporting all types of onsite monitoring visits.
• Performing CRF reviews, source data 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.

Connaissances

Dutch & English fluency

French proficiency

Driver's license

Willingness to travel

On-site monitoring in Belgium

Monitoring visits (Phase II/III)

Formation

BSc or MSc in Life Sciences

Outils

MS Office

Description du poste

Freelance Senior Clinical Research Associate

• Full-time

PSI is a leading Contract Research Organisation with 30 years in the industry, offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications.

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 beon subjects’ rights, safety and well-being and quality of data compliance.

This is a freelance (contractor) position in Belgium.

Your main responsibilities will include:

• 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
• Supervisingstudy 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

• BSc or MSc in Life Sciences (or similar),or an equivalent combination of education, training & experience
• Independent on-site monitoring experience in Belgium, ideally onmultiple projects at a time
• Demonstrable experience in all types of monitoring visits in Phase II and/or III
• Experience supporting Oncology/ Hematologyand Infectious disease studies
• Fluencyin 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