In-House Clinical Research Associate

Site In-House Clinical Research Associate

Location: Remote, Belgium

Travel: Up to approximately 50%

We are looking for an experienced Site In-House CRA II, based in Belgium, to support clinical studies at assigned sites. Working closely with the Site Management team, you will help sites start on time, maintain protocol and regulatory compliance, and complete study closeout activities.

Responsibilities

• Coordinate site startup, maintenance and closeout, acting as a primary contact for assigned sites.
• Review informed consent forms, study data and regulatory documents for accuracy and completeness.
• Support data query resolution and follow up on findings from monitoring visits and audits.
• Work with study teams and site personnel to resolve protocol-related issues, escalating where needed.
• Maintain clinical trial information and document management systems.
• Support training, mentor less experienced team members and contribute to process improvements.

Requirements

• At least five years of clinical research experience, or an equivalent combination of education and experience.
• A bachelor’s degree, preferably in natural science, nursing, pre-medicine or bioengineering.
• Strong knowledge of clinical trial processes and regulatory requirements.
• The ability to manage site relationships, interpret basic clinical data and work with limited supervision.
• Strong communication, organisational and Microsoft Office skills.
• Ability to travel up to approximately 50%.

SoCRA or ACRP certification would be an advantage.

Interested? Apply through LinkedIn with your CV.