Senior Clinical Research Associate — Remote/Hybrid

CTI Clinical Trial and Consulting Services; Brussel; Hybride; EUR 60 000 - 85 000; Plein temps

Avantages offerts par ce poste

Hybrid work from home opportunities

Résumé du poste

CTI Clinical Trial and Consulting Services is seeking an experienced Clinical Research Associate to oversee monitoring activities at assigned study sites. The role includes site visits, regulatory document handling, and collaboration with sponsors and project teams to ensure quality and timelines.

You will contribute to study start-up, patient enrollment strategies, and IP accountability while maintaining regulatory compliance across trials. Hybrid work options may be available.

Qualifications

• Minimum 3 years of clinical trial monitoring experience.
• Fluent in English.
• Bachelor's degree or higher in allied health, life sciences, or nursing.
• Experience in conducting clinical research studies in hospital settings, pharmaceutical companies, or CRA roles.

Responsabilités

• Serve as main CTI contact for assigned study sites.
• Conduct site visits (PSV, SIV, IMV, COV) and complete site visit deliverables with quality within Monitoring Plan timelines.
• Assist with or oversee study start-up activities, including feasibility and site selection.
• Collect, review and track essential/regulatory documents.
• Participate in general and study-specific training as required.
• Participate in investigator, client and project team meetings; may include presentations.
• Create and implement subject enrollment strategies for assigned study sites.
• Ensure proper storage, dispensation and accountability of Investigational Product and trial-related materials.
• Perform site management activities and provide updates of site status to Clinical Project Manager.

Connaissances

Clinical trial monitoring

Regulatory understanding

Formation

Bachelor's degree or higher in life sciences

Description du poste

CTI Clinical Trial and Consulting Services is seeking an experienced Clinical Research Associate to oversee monitoring activities at assigned study sites. The role includes site visits, regulatory document handling, and collaboration with sponsors and project teams to ensure quality and timelines.

You will contribute to study start-up, patient enrollment strategies, and IP accountability while maintaining regulatory compliance across trials. Hybrid work options may be available.