meeting protocol

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;...

pAegis Vision is seeking a seasoned penetration tester to conduct comprehensive testing of web applications, IT infrastructure, and application-level security using defined methodologies. You will assess vulnerabilities across OS, software, protocols, and networks, delivering actionable mitigations and clear risk analyses. /ppYou will participate in kickoff...

Jobtailor in Belgium is seeking a Clinical Operations Assistant to support monitoring activities, maintain the Trial Master File (TMF) and project files, and assist with site management tasks. You will coordinate documentation, prepare site manuals and reference tools, manage incoming and outgoing regulatory documents, and support team meetings to ensure...

Aegis Vision is seeking a seasoned penetration tester to conduct comprehensive testing of web applications, IT infrastructure, and application-level security using defined methodologies. You will assess vulnerabilities across OS, software, protocols, and networks, delivering actionable mitigations and clear risk analyses.You will participate in kickoff...

Job Description Summary The Medical Monitor, Clinical Development is responsible for providing day‑to‑day medical oversight for one or more clinical trials to ensure patient safety, data integrity, and protocol compliance throughout trial execution. This role serves as the primary medical point of contact for study teams and clinical sites, supporting...

The EORTC medical department is looking for a Medical Liaison Officer (MLO) to reinforce its team. The Medical Liaison Officer works under the hierarchical supervision of Head of Medical Department or delegate. Objective The Medical Liaison Officer serves as the primary point of contact for disease-oriented groups or cross-discipline committees, overseeing...

Job Description Summary The Medical Monitor, Clinical Development is responsible for providing day‑to‑day medical oversight for one or more clinical trials to ensure patient safety, data integrity, and protocol compliance throughout trial execution. This role serves as the primary medical point of contact for study teams and clinical sites, supporting...

Reports to the Supervisor QA (A.I.)ObjectivesAs a Senior Quality Engineer, you safeguard quality levels by monitoring and ensuring that all operations at all levels are carried out in accordance with the cGMP quality systems applied within Prothya Biosolutions. In this way, you contribute to Prothya Biosolutions’s pharmaceutical products meeting European...

When our values align, there's no limit to what we can achieve. About ParexelParexel is a leading global clinical development partner delivering insight-driven clinical and consulting solutions to the life sciences industry. With 22,000+ employees worldwide, we partner with biopharmaceutical companies and research sites to design and deliver patient-focused...

About Parexel Parexel is a leading global clinical development partner delivering insight-driven clinical and consulting solutions to the life sciences industry. With 22,000+ employees worldwide, we partner with biopharmaceutical companies and research sites to design and deliver patient-focused clinical trials that broaden access and make research a care...

Key Responsibilities1. Hospitality & ExperienceDeliver a consistently warm and professional welcome.Ensure spaces are always guest-ready (cleanliness, layout, supplies, atmosphere).Handle member requests and resolve issues efficiently.Manage mail, deliveries, and visitor check-in.2. Operations & CoordinationMonitor stock levels, supplies, and facility...

En tant que Coordinateur de Recherche clinique en hépato-gastroentérologie et pour l'Unité de Pharmacologie clinique, vous êtes en charge des responsabilités suivantes :Vous travaillez au sein d'une équipe pluridisciplinaire et interagissez avec les différents acteurs de la recherche clinique, dans le respect des « Good Clinical Practice »;Vous...

At Allucent™, we are dedicated to helping small-medium biopharmaceutical companies efficiently navigate the complex world of clinical trials to bring life-changing therapies to patients in need across the globe.We are looking for a Sr. Clinical Data Manager (SrCDM) to join our A-team (hybrid*/remote). As a SrCDM at Allucent you lead data management...

Analytical Method Validation SpecialistEurofinsWavre, BelgiumKey ResponsibilitiesAnalytical Method Validation DocumentationAuthor and maintain validation-related documentation including:Validation protocols.Validation reports.Amendments.Risk assessments.Scientific rationale reports.Technical instructions.Periodic review documentation.Raw data review...

Penetration Testing Execution: Provide comprehensive web application, IT infrastructure, and application-level testing (including COTS and GOTS software) using defined methodologies . Vulnerability & Risk Analysis: Assess security vulnerabilities within operating systems, software, protocols, and networks; evaluate risks and formulate actionable...

Job Overview The Medical Director for the Hematology-Oncology Center of Excellence provides strategic medical and scientific subject matter input to IQVIA in this therapeutic area informed by their training, experience and expertise. The activity of the medical director includes but is not necessarily limited to early engagement with potential customers,...

At Allucent™, we are dedicated to helping small-medium biopharmaceutical companies efficiently navigate the complex world of clinical trials to bring life-changing therapies to patients in need across the globe. We are looking for a Sr. Clinical Data Manager (SrCDM) to join our A-team (hybrid*/remote). As a SrCDM at Allucent you lead data management...

Sr. Clinical Research Associate - Belgium (French & Dutch Fluency)Alimentiv is a global CRO with a singular focus: advancing therapies for patients with gastrointestinal diseases. GI is our WHY and for more than 30 years that purpose has driven our scientific rigour, operational excellence, and deep therapeutic expertise, including supporting more than 70%...

En tant que Coordinateur de Recherche clinique en hépato-gastroentérologie et pour l'Unité de Pharmacologie clinique, vous êtes en charge des responsabilités suivantes :Vous travaillez au sein d'une équipe pluridisciplinaire et interagissez avec les différents acteurs de la recherche clinique, dans le respect des « Good Clinical Practice »;Vous...

Bu bir uzaktan pozisyondur.About UsWellbees is a wellbeing platform that creates a positive impact on both personal and organizational transformation by combining the power of social interaction with expert support, company-specific activities, content across eight wellbeing categories, and more.Wellbees currently serves more than 215,000 employees across...