Planet Pharma are currently partnered with a global pharmaceutical company and we are actively seeking a Clinical Research Associate I to join the business on a permanent basis in Belgium.
Key Responsibilities:
* Monitor clinical trial sites to ensure studies are conducted in compliance with ICH-GCP, protocol requirements, and regulatory guidelines.
* Perform site initiation, monitoring, and close-out visits (on-site and/or remote).
* Verify source data and case report forms (CRFs) to ensure accuracy, completeness, and data integrity.
* Ensure patient safety and rights are protected throughout the study.
* Review and track adverse events (AEs/SAEs) and ensure proper reporting.
* Maintain essential study documentation, including Trial Master File (TMF) and Investigator Site Files (ISF).
* Train and support site staff on study protocols and procedures.
* Ensure timely resolution of data queries and protocol deviations.
* Collaborate with project managers, data management, and regulatory teams to support study progress.
* Prepare and submit detailed monitoring visit reports.
* Assist with site selection, feasibility assessments, and regulatory submissions where required.
* Track study timelines and recruitment targets to ensure milestones are met.
Key Requirements:
* Must speak French, Dutch & English (essential)
* Oncology experience (preferred)
* Phase I study experience (preferred)
About Planet Pharma:
Planet Pharma is an American parented Employment Business/Agency that provides global staffing services with its head-quarters in Chicago and our EMEA regional office located in Central London. We have invested significantly in creating a robust international platform that enables us to work compliantly in 30+ countries with a current network of 2500+ active contractors globally as well as a very strong permanent / direct hire recruitment offering.
Our specialist knowledge and close relationships with our clients and the wider industry really makes us unique in our field. Just recently we were recognised by FORBES as the 17th best professional staffing firm, and have won multiple awards from industry accredited bodies for our commitment to excellence and service delivery. We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing.
We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of their race, sex, disability, religion/belief, sexual orientation or age.
www.planet-pharma.com
Please click 'apply' or contact Harry Banks at Planet Pharma for more information:
E: hbanks@planet-pharma.co.uk