Freelance Senior Clinical Research Associate

Psi-Cro; Brussel Hoofdstad; Sur place; EUR 55 000 - 85 000; Plein temps

Résumé du poste

PSI is a leading Contract Research Organisation seeking a Senior Freelance Clinical Research Associate in Belgium. You will lead onsite monitoring visits, review CRFs, and ensure data quality while maintaining strong site relationships and study timelines.

Fluency in Dutch and English, proficiency in French, and willingness to travel are required, along with a life sciences degree and prior on-site monitoring experience in Phase II/III trials.

Qualifications

• BSc or MSc in Life Sciences (or equivalent) required.
• Independent on-site monitoring experience in Belgium, ideally on multiple projects.
• Experience with Phase II/III monitoring visits and data quality.
• Fluent in Dutch and English; professional proficiency in French.
• Full and clean driver’s license; ability to travel.

Responsabilités

• Conducting and reporting onsite monitoring visits.
• Performing CRF reviews, source data verification and query resolution.
• Managing site communication and relationships with investigators.
• Supervising study activities, timelines and schedules per site.
• Supporting quality control through compliance monitoring and reports review.

Connaissances

On-site monitoring

Site communication

Travel willingness

Quality/compliance focus

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