other
Posted 16 hours agoCRA I
at Fortrea
BelgiumRemote
Requirements
- Qualifications University degree in a related life sciences or health field, or equivalent relevant experience.
- Basic knowledge of regulatory guidelines and clinical trial processes.
- Fluency in English and the local office language (For Netherlands: Dutch, for Belgium: Dutch and French).
- Proficiency with standard computer applications.
- Ability to work effectively in a matrix environment.
- Valid driver’s license. What We Offer Opportunities to grow your career in a global clinical research environment.
Experience
- At least 6 months of independent monitoring experience.
Additional details
- Join Fortrea as a Clinical Research Associate I and contribute to the delivery of high‑quality clinical trials that make a real difference in patients’ lives.
- This role offers an exciting opportunity to build your monitoring expertise while working in a dynamic, global life sciences environment that drives innovation and advances healthcare worldwide.
- This role is critical in ensuring clinical studies are executed with excellence, safeguarding patient safety and data integrity while supporting the successful delivery of impactful research programs.
- This role is for upcoming future opportunities that may arise at Fortrea. Key
- Responsibilities You will conduct all aspects of study site monitoring, including routine visits, initiation, and close‑out activities.
- You will oversee site management activities in alignment with project plans and SOPs.
- You will ensure study staff are properly trained and equipped to conduct the protocol safely and accurately.
- You will safeguard patient safety by verifying informed consent and adherence to protocol and regulatory requirements.
- You will review source documentation to ensure data integrity and identify missing or inconsistent data.
- You will manage monitoring tasks efficiently and in line with Fortrea policies, including economical travel planning.