Do you have a scientific background and 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 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
- Degree in Life Sciences.
- At least one prior professional experience in clinical research (industry, CRO, or hospital environment) is required. Hands-on experience with clinical trial processes is necessary.
- Good understanding of clinical trial processes and GCP guidelines.
- Fluency in English and in any other 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 Brussels (1 day of homeworking/week after 3 months)
- A balanced salary package based on your capabilities and experience, including extra-legal benefits.
