clinical study assistant

Position: Local Study Operations Line ManagerLet’s do this. Let’s change the world. In this role, you will lead the skill development of Local Study Operations Managers, ensuring effective trial implementation within the country and strong alignment with global strategies. You will oversee the delivery of the country’s study portfolio—managing scope,...

About Cogstate At Cogstate, we’re advancing the science of brain health - making it faster, easier, and more accurate to assess cognition across clinical trials, healthcare settings, and everyday life. Our digital cognitive assessments are trusted by researchers, clinicians, and pharmaceutical partners around the world, helping to drive breakthroughs in...

Make your mark for patients We are looking for a Global Head of Clinical Program Delivery who is collaborative, strategic and patient-focused to join our Global Clinical Operations team, based either at our Belgium headquarters or in Windlesham, UK. This global role requires approximately 25–30% travel to support collaboration across locations and with...

PSI CRO is seeking a Freelance Senior Clinical Research Associate in Belgium to lead on-site monitoring, ensure data quality and compliance, and maintain timely study milestones.You will manage site communications, perform source data verification, support vendors, and coordinate monitoring visits across Phase II/III oncology, hematology, and infectious...

Serve as main CTI contact for assigned study sites Conduct site visits (pre-study [PSV], site initiation [SIV], interim monitoring [IMV], and close-out [COV]) and complete site visit deliverables with quality and within given timelines in Monitoring Plan while adhering to all applicable regulatory requirements, SOPs and ICH GCP Assist with or oversee study...

Serve as main CTI contact for assigned study sites Conduct site visits (pre-study [PSV], site initiation [SIV], interim monitoring [IMV], and close-out [COV]) and complete site visit deliverables with quality and within given timelines in Monitoring Plan while adhering to all applicable regulatory requirements, SOPs and ICH GCP Assist with or oversee study...

ICON Strategic Solutions is recruiting a Senior Clinical Trial Manager to lead trial delivery across global programmes. You will manage operations, resolve issues, and build team capability within a sponsor-dedicated model.You will oversee budgets, monitoring plans, and study start-up activities while coaching Clinical Research Associates to improve...

## Experienced Clinical Research Associate, Multi-Sponsor, BelgiumApplylocations: Brussels, Brussels-Capital Region, Belgiumtime type: Full timeposted on: Posted Todayjob requisition id: R1552876***Clinical Research Associate***IQVIA Belgium is looking for talented and motivated experienced CRA to join our Site Management team. At this position you...

Independently performs, coordinates and oversees all aspects of the clinical site monitoring services, assessing protocol and regulatory compliance as per Alimentiv’s and sponsor’s standard processes, ICH/GCP guidelines and local regulation. Serves as the primary liaison between the sponsor/Alimentiv and investigative sites by playing a critical role in...

European Clinical Training & Demo Manager located at ORSI Academy, Belgium.Position OverviewWe are seeking an experienced and highly organised European Clinical Training & Demo Manager to lead and coordinate customer training and customer demonstrations at the ORSI Academy, in Belgium.The Clinical Surgical Robotics Trainer is responsible for delivering...

TFS HealthScience is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includes full service-capabilities, resourcing and Functional Service (FSP) solutions. Join Our Team as a Freelance Senior Clinical Research...

Independently performs, coordinates and oversees all aspects of the clinical site monitoring services, assessing protocol and regulatory compliance as per Alimentiv’s and sponsor’s standard processes, ICH/GCP guidelines and local regulation. Serves as the primary liaison between the sponsor/Alimentiv and investigative sites by playing a critical role in...

Independently performs, coordinates and oversees all aspects of the clinical site monitoring services, assessing protocol and regulatory compliance as per Alimentiv’s and sponsor’s standard processes, ICH/GCP guidelines and local regulation. Serves as the primary liaison between the sponsor/Alimentiv and investigative sites by playing a critical role in...

IQVIA Belgium is seeking a Clinical Research Associate to perform monitoring and site management, ensuring compliance with study protocols. The role involves conducting site visits, recruiting subjects, and maintaining communication with study sites.The ideal candidate holds a relevant degree and has at least 2 years of CRA experience. Strong organizational...

4G Clinical is seeking a Backend Software Engineer to advance our Python/Django backend, focusing on safe, scalable solutions for clinical trial data and workflows. You will implement study-specific reports, data scripts, and client integrations with external APIs.The role requires 5+ years in a related field, strong communication, and willingness to travel...

Clinical Research Associate IQVIA Belgium is looking for talented and motivated CRA to join our Site Management team. At this position you will have the opportunity to put your passions to work in an environment designed to help you gain experience in a wide variety of therapeutic areas, and build a meaningful, strong career within our organization. Perform...

A leading clinical trials organization is seeking a full-time Project Coordinator in Leuven, Belgium. The role involves maintaining study-related documents, coordinating laboratory shipments, and serving as a primary contact for study teams. Ideal candidates should hold a Bachelor's degree in life sciences and demonstrate excellent organizational and...

Excelya is seeking a highly organized clinical operations professional to coordinate trials across sites and countries, ensuring regulatory compliance and timely execution.You will manage TMF, trial documentation, study systems, and cross-functional communication, contributing to a high-quality patient journey. This role offers exposure to global studies and...

Clinical Research Associate IQVIA Belgium is looking for talented and motivated CRA to join our Site Management team. At this position you will have the opportunity to put your passions to work in an environment designed to help you gain experience in a wide variety of therapeutic areas, and build a meaningful, strong career within our organization. Perform...

Job SummaryMedpace is the leading CRO for Biotech companies and is continuing to add Clinical Trial Managers of different experience levels to join our Clinical Trial Management Group in Belgium, Leuven. Clinical Trial Managers with expertise in Oncology/Cardiovascular/Endocrine/Metabolic are welcome to continue to work in their area of expertise or to...