Senior CRA & Mentorship Lead – Hybrid/Remote Options

Ctifacts; Belgique; Hybride; EUR 42 000 - 62 000; Plein temps

Avantages offerts par ce poste

Hybrid work from home opportunities

Career development programs

Global exposure

Résumé du poste

CTI Clinical Trial and Consulting Services is seeking a seasoned clinical trial monitor to lead monitoring activities across assigned sites. You will ensure regulatory compliance, manage source data verification, and collaborate with cross-functional teams to drive trial quality and timelines.

The role includes site visits (PSV, SIV, IMV, COV), start-up support, and ongoing mentoring for CRAs within a global CRO framework. Hybrid work options may be available in Belgium.

Qualifications

• Minimum 3 years of clinical trial monitoring experience or equivalent per CTI requirements.
• Bachelor's degree or higher in nursing, pharmacy or allied health; RN with required experience acceptable.
• Experience conducting clinical studies in hospital, pharmaceutical or CRO environments.

Responsabilités

• Serve as main CTI contact for assigned study sites.
• Conduct PSV, SIV, IMV and COV visits with timely, quality deliverables.
• Assist with study start-up activities including feasibility and site selection.
• Collect, review and track essential/regulatory documents.
• Monitor site status and lead CRA training and mentoring.
• Oversee IP storage, dispensation and accountability.
• Collaborate with Regulatory Affairs and Ethics Committees as needed.
• Create subject enrollment strategies and support data management activities.

Connaissances

Clinical trial monitoring

GCP compliance

CRO experience

Formation

Bachelor's degree or higher in allied health or nursing

RN with Associate's Degree

3-year Nursing Diploma with clinical nursing experience

Description du poste

CTI Clinical Trial and Consulting Services is seeking a seasoned clinical trial monitor to lead monitoring activities across assigned sites. You will ensure regulatory compliance, manage source data verification, and collaborate with cross-functional teams to drive trial quality and timelines.

The role includes site visits (PSV, SIV, IMV, COV), start-up support, and ongoing mentoring for CRAs within a global CRO framework. Hybrid work options may be available in Belgium.