clinical study

Job Summary Medpace is currently seeking candidates with Radiopharmaceutical or Nuclear Medicine PhDs and/or Post-Doctoral Research experience for a full-time, office-based Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team. The aCTM will be a part of the Clinical Trial Management team working with Project Coordinators and...

Job SummaryMedpace is currently seeking candidates with Oncology related PhDs and/or Post-Doctoral Research experiencefor a full-time, office-based Associate Clinical Trial Manager (aCTM) to join our Belgium, Leuven Clinical Trial Management team. The aCTM will be a part of the Clinical Trial Management team working with Project Coordinators and Clinical...

Medpace in Belgium (Vlaams-Brabant) seeks Medical Directors to provide medical, scientific, and strategic leadership for planning, execution, and reporting of clinical trials. Serve as the internal medical expert for study design, protocols, and project plans. Responsibilities include medical management, safety oversight, and collaboration across...

Medpace in Belgium (Vlaams-Brabant) seeks Medical Directors to provide medical, scientific, and strategic leadership for planning, execution, and reporting of clinical trials. Serve as the internal medical expert for study design, protocols, and project plans.Responsibilities include medical management, safety oversight, and collaboration across departments;...

We are the people who give possibilities purpose BD is one of the largest global medical technology companies in the world. Advancing the world of health™ is our Purpose, and it’s no small feat. It takes the imagination and passion of all of us—from design and engineering to the manufacturing and marketing of our billions of MedTech products per...

Senior Clinical Trial Management At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise. As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that...

Medpace in Leuven, Belgium is seeking an Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team on a full-time, office-based basis. The role involves supporting global study activities alongside Project Coordinators and Clinical Trial Managers, applying analytical and academic skills to clinical project administration and...

Syneos Health is seeking a Global Study Manager (Oncology) / Senior Project Manager for sponsor-dedicated, EMEA regions in Belgium. Lead cross-functional clinical trials, ensuring GCP compliance and on-time delivery while managing budgets and client expectations.You will mentor PMs, oversee trial plans, and collaborate with stakeholders across regions to...

ICON Strategic Solutions is seeking a Senior Clinical Trial Manager to oversee clinical trial operations and support the team and stakeholders across programmes. You will focus on coordinating delivery, resolving issues, and building team capability.The role includes budget oversight, monitoring plan development, CRA mentoring, and driving study start-up and...

IQVIA Biotech is a unique division specialising in working with smaller biotech and emerging biopharma clients and as such we have a vibrant, fast-paced working environment. The sector we are in is cutting edge for therapies with un-met medical need. IQVIA Biotech has an exciting position within its EU Clinical Monitoring team. The Clinical Monitoring...

Join us as we transform immunology and deliver medicines that help autoimmune patients get their lives back. argenx is preparing for multi-dimensional expansion to reach more patients through a rich pipeline of differentiated assets, led by VYVGART, our first-in-class neonatal Fc receptor blocker approved for the treatment of gMG, and with the potential to...

UCB is seeking a Senior Principal Programmer to join the Programming, Visualization and Reporting team, with offices in Brussels, Monheim, Raleigh or Slough. This role supports moving clinical programming to a modern Statistical Computing Environment in a hybrid work model.You will translate reporting needs into well-governed study setups, support compliant...

Your mission: As a Clinical Project Manager at Cascador/moveUP, you will be responsible for the management of the clinical trials of our partners, ensuring their smooth progress and managing upcoming clinical trials, with the use of our next-generation eCOA/eDiary Platform. You will be in direct contact with our sponsors, academic centers and sites using our...

Questa posizione è in IQVIAIl processo di selezione sarà interamente gestito IQVIA.Questa opportunità è disponibile in Reading - United Kingdom, Belgrade - Serbia, Budapest - Hungary, Barcelona - Spain, Berlin - Germany, Sofia - Bulgaria, Bellville - South Africa, Bucuresti - Romania, Milan - Italy, Madrid - Spain, Lisbon - Portugal, Brussels - Belgium,...

Alimentiv 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 sponsor/Alimentiv and investigative sites by playing a critical...

Are you an experienced freelance CRA and have full-time availability for a project to start asap? You will be welcomed in a global company in which team spirit is key. Job Description As a Senior CRA, you will work on the frontline of communication with project stakeholders, ensuring timelines, targets and standards of clinical research projects in a variety...

IQVIA is seeking a Clinical Independent Rater who is Turkish-speaking to review clinical trial scales, engage in methodology discussions, and support rater performance. This remote, part-time role requires 10–16 hours per month and involves training, data review, and live interchanges with raters to ensure scoring accuracy.The position emphasizes adherence...

Oxford Global Resources seeks a Clinical Research Associate to monitor clinical investigations for medical devices at Brussels-area sites. The CRA will ensure patient safety, data integrity and protocol compliance, and act as the primary liaison with investigators and study staff.The role requires up to 80% travel, onsite presence in Brussels at least once...

Fortrea is seeking a Lead CRA based in Belgium to manage site monitoring activities for clinical studies in line with ICH GCP, SOPs and sponsor requirements. You will ensure subject protection, data integrity, regulatory document completeness, and audit readiness across sites.The role involves 60% travel to study sites, coordinating with the study team,...

Pauwels Consulting seeks a Clinical Research Associate to oversee clinical activities across study sites for medical device projects. You will monitor sites, ensure data quality, and manage regulatory compliance with GCP and SOPs. Travel up to 80% to investigator sites is required.Fluency in English and Dutch, a life sciences degree, and 2+ years in clinical...