Clinical Research Associate (CRA)

Biopark; Louvain-la-Neuve; Remote; EUR 50,000 - 65,000; Full time

Job summary

Biopark is seeking a Clinical Research Associate (CRA) Inteliphage to support the conduct of clinical trials, ensuring protocol compliance and data integrity. You will monitor sites, coordinate with investigators and internal teams, and help translate scientific work into reliable patient solutions.

The role combines scientific rigor with project coordination, covering site initiation, monitoring visits, data verification, and maintenance of trial master files, while upholding ICH-GCP and

Qualifications

• Master’s degree in life sciences, pharmacy, biotechnology, clinical research, or a related field.
• Experience in clinical research, ideally with interventional or observational studies.
• Strong knowledge of ICH-GCP standards, regulatory requirements, and clinical trial processes.
• Experience in clinical monitoring, site management, or study coordination.
• Excellent organizational skills, rigor, and ability to manage priorities.
• Strong autonomy, with ability to work in a team and interact with stakeholders.
• Excellent written and verbal communication skills.

Responsibilities

• Monitoring, coordinating, and following up on clinical trials in accordance with study protocols.
• Ensuring compliance with ICH-GCP standards, internal procedures, and applicable regulatory requirements.
• Preparing and conducting site selection, initiation, monitoring, and close-out visits.
• Managing relationships with investigators, clinical site teams, and involved partners.
• Verifying the quality, consistency, and accuracy of collected data.
• Identifying, documenting, and following up on deviations, observations, or required corrective actions.
• Writing monitoring reports and ensuring rigorous follow-up of ongoing actions.
• Contributing to study-related documentation and trial master file activities.
• Collaborating with internal teams, including clinical operations, quality, regulatory affairs, data management, and operations.

Skills

Clinical monitoring

Site management

Regulatory compliance

Data quality

ICH-GCP

Stakeholder communication

Documentation

Education

Master’s degree in life sciences or related field

Job description

Clinical Research Associate (CRA) Inteliphage

At the heart of clinical trials, you play an essential role in ensuring the smooth conduct of studies, compliance with regulatory requirements, and the quality of collected data.As a Clinical Research Associate, you work closely with investigators, clinical sites, internal teams, and external partners to ensure studies are conducted with rigor and reliability.Your mission: to help transform scientific research into concrete, reliable, and accessible therapeutic solutions for patients.

You are responsible for the operational monitoring of clinical trials, from site initiation through to site close-out. You ensure compliance with study protocols, Good Clinical Practice, and applicable regulatory requirements.

Your role is scientific, operational, and relationship-driven: you safeguard data quality, support investigator sites, and contribute to the overall success of clinical studies.

Your responsibilities

You will be responsible for:

• Monitoring, coordinating, and following up on clinical trials in accordance with study protocols
• Ensuring compliance with ICH-GCP standards, internal procedures, and applicable regulatory requirements
• Preparing and conducting site selection, initiation, monitoring, and close-out visits
• Managing relationships with investigators, clinical site teams, and involved partners
• Verifying the quality, consistency, and accuracy of collected data
• Identifying, documenting, and following up on deviations, observations, or required corrective actions
• Writing monitoring reports and ensuring rigorous follow-up of ongoing actions
• Contributing to study-related documentation and trial master file activities
• Collaborating with internal teams, including clinical operations, quality, regulatory affairs, data management, and operations

Your profile

You ideally bring:

• A Master’s degree in life sciences, pharmacy, biotechnology, clinical research, or a related field
• Experience in clinical research, ideally with interventional or observational studies
• A good understanding of ICH-GCP standards, regulatory requirements, and clinical trial processes
• Experience in clinical monitoring, site management, or study coordination
• Excellent organizational skills, rigor, and ability to manage priorities
• Strong autonomy, combined with the ability to work as part of a team and interact with various stakeholders
• Excellent written and verbal communication skills
• An analytical mindset and strong attention to data quality

What we offer

By joining the team, you will benefit from:

• Clinical projects with strong scientific and therapeutic impact
• A key role in the development of innovative healthcare solutions
• An international, structured, and collaborative environment
• Continuous training and opportunities to develop relevant certifications
• A work culture based on quality, trust, and responsibility
• A healthy work-life balance
• Concrete responsibilities and genuine autonomy within your scope

Why join this role?

This position is ideal for a rigorous, organized, and communicative professional who wants to contribute directly to the success of demanding clinical trials.

You will join an environment where quality, compliance, and strong site relationships are central to success, with one shared objective: advancing clinical research for the benefit of patients.