Senior Clinical Research Associate (Clinical Research)

Location: Home based in Belgium; the role is listed in Zaventem and includes on-site monitoring visits at Belgian study sites.

Company

hirify.global provides clinical research services, healthcare intelligence, data, technology, and analytics for life sciences and healthcare organizations.

What you will do

• Conduct site selection, initiation, monitoring, and close-out visits in line with the contracted scope, GCP, ICH, and applicable regulations.
• Support site recruitment plans, track enrollment, and manage protocol and study training.
• Evaluate study-site quality and protocol compliance, escalating issues when appropriate.
• Track regulatory submissions, approvals, CRF completion, data queries, and study progress.
• Maintain TMF and ISF documentation and prepare monitoring reports, follow-up letters, and action plans.
• Collaborate with project managers, study coordinators, investigators, and cross-functional global teams.

Requirements

• University degree in a scientific or healthcare discipline.
• At least 3 years of independent, on-site CRA monitoring experience in a CRO or pharmaceutical environment.
• Excellent written and spoken Dutch, French, and English.
• Strong knowledge of clinical research regulations, GCP, and ICH guidelines.
• Organizational, problem-solving, interpersonal, and cross-cultural communication skills.
• Ability to build trusted partnerships with Belgian investigators and medical staff and collaborate with global teams.

Culture & Benefits

• Access to career development resources, training, and advancement opportunities.
• Dedicated learning and development programs to expand therapeutic knowledge.
• Flexible working arrangements supporting professional and personal commitments.
• Company car, mobile phone, and a rewards and benefits package.
• A supportive culture within a global clinical research organization.