Senior Clinical Research Associate, French, Dutch Fluency

This is a fully remote position, open to applicants in Belgium.

📋 Description

• Oversee, deliver, and/or execute comprehensive clinical site monitoring services for one or more projects.

• Design and manage project monitoring services, which include training, recruitment of sites/patients, management of site data/documents, oversight of project site budgets, and regulatory submissions.

• Ensure that all activities comply with SOPs, study protocols, and GCP best practices.

• Serve as the primary point of contact between CRAs and the project team in the capacity of Lead CRA.

• Engage in the development of project plans, protocols, CRFs, communications, monitoring forms, documents, and tools.

• Foster collaborative relationships with all stakeholders involved.

• Act as a subject matter expert, providing mentorship, coaching, and performance feedback to colleagues.

• Assist with the selection, hiring, training, and supervision of CRAs; conduct co-monitoring and training visits.

• Act as the escalation point for issues related to sites/patients and concerns from Sponsors.

• Identify and recruit site investigators, ensuring the proper delivery of trial materials and documents.

• Enhance patient recruitment strategies and offer guidance on inclusion/exclusion criteria.

• Function as the primary clinical site contact, ensuring the integrity of the study.

• Facilitate site access to study systems and ensure compliance with project-specific training.

• Monitor site-related issues until they are fully resolved.

• Coordinate clinical-site communications with project teams throughout the project's lifecycle.

⛳️ Requirements

• A minimum of a college diploma or degree.

• 4–6 years of relevant experience.

• Excellent communication skills.

• Self-motivated with a strong commitment to achieving positive outcomes.

• Exceptional attention to detail.

• Capacity to build collaborative relationships.

• Strong critical thinking skills.

• Willingness to travel regularly to clinical sites.

• Fluency in English, Dutch, and French is required.

• Familiarity with and application of SOPs, study guidelines, and GCP best practices.

🏝️ Benefits

• One-time sign-on bonus of €3,000.

• Annual Bonus (Short Term Incentive Program) with a target of 8% of annual salary.

• Monthly stipend of €157.83 to cover business communication expenses.

• Monthly mobile phone stipend of €40.

• One-time reimbursement of up to €500 for office supplies.

• Mileage reimbursement for travel.