Clinical Study Docs

Are you highly organized, detail-oriented, and interested in contributing to clinical research? Do you have a first experience in clinical research? Then this is a great opportunity for you! We are looking for a Clinical Study Assistant to provide administrative and operational support to study teams throughout the lifecycle of clinical studies.Presence at...

Oxford Global Resources in Belgium is seeking a Clinical Study Assistant to provide administrative and operational support to study teams throughout the lifecycle of clinical studies. Presence at the client’s location (north of Brussels) is required.You will help maintain study documentation, prepare regulatory binders, and support QA, site audits, and...

Planet Pharma is seeking a Clinical Editor to join a global leader in medical communications. This remote, contract role focuses on precision, accuracy, and regulatory compliance of clinical documents in English.You will edit for clarity, perform fact-checks, and collaborate with medical writers to ensure documents are inspection-ready and audit-ready. You...

Planet Pharma is seeking a Clinical Editor to join a leading medical communications team in Belgium. You will ensure accuracy, consistency, and regulatory compliance of clinical documents, perform fact checks, edit for clarity, and prepare content for inspection-readiness.This role rewards meticulous editors with strong English language skills, AMA style...

EORTC is looking for a Junior Clinical Operations Manager (JrCOM) to reinforce its team.The junior Clinical Operations Manager works under the hierarchical supervision of Head of the Clinical Operations Department.ObjectiveThe objective of the Junior Clinical Operations Manager at EORTC is to support the planning, coordination, and execution of clinical...

EORTC, the European Organisation for Research and Treatment of Cancer, invites applications for a Junior Clinical Operations Manager who will support planning, coordination, and execution of clinical studies under the Head of the Clinical Operations Department.You will assist with study setup, monitoring timelines, and maintaining quality across activities...

Clinical Research Coordinator in TurnhoutWorking Hours: 8-10 hours per week Start Date: Immediately Duration: Approximately 9 monthsKey ResponsibilitiesPrescreening and Screening tasksReview charts from the site data baseMaintaining and updating study documentation, including protocols, case report forms (CRFs), Electronic Data Capture (EDC) systems and...

Join Excelya, where Audacity, Care and Energy define who we are and how we work. We believe in creating ambitious solutions and fostering an inclusive environment where collaboration and individual growth go hand in hand. We are looking for a Clinical Trial Assistant to support the successful planning, execution and oversight of clinical trials across...

Join Excelya, where Audacity, Care and Energy define who we are and how we work. We believe in creating ambitious solutions and fostering an inclusive environment where collaboration and individual growth go hand in hand. We are looking for a Clinical Trial Assistant to support the successful planning, execution and oversight of clinical trials across...