Inhouse CRA Brussel (BE) • Oxford Global Resources

Vacature in het kort

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Do you have a scientific background and a first experience in clinical trials? Are you fluent in English and in another European language? Do you have strong planning, communication and multitasking skills ? Are you quickly available and open for an office-based position in the area of Brussels? Then check out the opportunity below.

Job description

As Inhouse CRA, you play a critical role in the planning and conduct of clinical trials, supporting the study team to ensure high-quality data collection, compliance with regulatory guidelines and adherence to study protocols.

Responsibilities

• Support the clinical project team in the planning and execution of clinical trials.
• Assist with site activation, follow-up and close-out activities remotely.
• Review and track essential regulatory documents.
• Maintain and update trial documentation and study management systems.
• Liaise with the internal study team and study sites to ensure timely start-up and proper conduct of the clinical trials.
• Assist in the preparation of study materials, reports, and presentations.
• Review of study-related documents such as Informed Consent Forms.
• Ensure compliance with ICH-GCP, SOPs, and all applicable regulations.

Requirements

• University degree in Life Sciences.
• Previous clinical research experience in the industry, academic or hospital environment.
• Good understanding of clinical trial processes and GCP guidelines.
• Fluency in English and in any other European language.
• Excellent communication, organizational and problem-solving skills.
• Ability to work collaboratively and independently when necessary.
• Existing right to work in Europe required.

Benefits

• Full-time position.
• Office-based role in the area of Brussels.
• A balanced salary package based on your capabilities and experience, including extra-legal benefits.