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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...

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...

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...

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 SUMMARY The Clinical Development Medical Senior Manager is accountable for the: Medical & scientific integrity of the study and well-being of participants enrolled in one or more clinical trials. Timely delivery of high-quality protocols and clinical study execution. Clinical data, safety, risk review and mitigation. Use of AI-enabled clinical...

Senior Engineer QA ValidationReports to the Supervisor QA Validation (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...

Principal Statistician - EMEA (Many Locations) - Sponsor-dedicated Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity, anticipate change and accelerate...

ppbPenetration Testing Execution: /bProvide comprehensive web application, IT infrastructure, and application-level testing (including COTS and GOTS software) using defined methodologies . /p /brpbVulnerability Risk Analysis: /bAssess security vulnerabilities within operating systems, software, protocols, and networks; evaluate risks and formulate...

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 mitigation...

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;...

moroww zoekt iemand die collecties vult en bewaakt voor vakantiehuizen met een label, en die dit proces hands-on uitvoert op locatie in België. Je belt eigenaren, bezoekt huizen en toetst het label volgens een strak protocol tot een handtekening is gezet.Je zegt vaker nee dan ja en combineert remote werk met 2-wekelijkse on-site meetings. Eén à twee dagen...

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...

We are searching for the best talent for a Product Quality Specialist to be based in Belgium, Netherlands, Ireland, or Italy.You will be responsible for:Has end-to-end accountability for the stability management and oversight from late stage development through full commercial lifecycle for a portfolio of products.Responsible for product quality related...

Responsibilities Perform activities in compliance with applicable Corporate and Clinical Operations Policies, Standard Operating Procedures and Work Instructions Assist Clinical Monitoring staff with site management activities, including serving as a Sponsor representative for sites on assigned studies, and communicating with sites to ensure compliance with...

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,...

Writing or coordinating clinical and regulatory documents such as, but not limited to, CSRs, IBs, protocols, summary documents, RMPs, regulatory responses, and briefing documents. Leading cross-functional (eg, with clinical team) document planning and review meetings. Interacting with cross-functional colleagues on document content and champions MW...

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 mitigation...

Author and coordinate regulatory medical writing documents supporting OncologyWrite and coordinate basic clinical documents, including Phase 1 protocols, Phase 1/2 CSRs, tables of studies, narratives, and initial IBsWrite, contribute to, and/or coordinate low- to medium-complexity clinical and regulatory documents, including Phase 2/3 CSRs and protocols, IB...

Who you are: The Center Director will lead the launch, establishment, and long-term management of the CIEE Brussels Center. This role requires a dynamic leader capable of building operations from the ground up while ensuring alignment with CIEE’s global standards.You will be responsible for center start-up, strategic planning, and operational execution,...

Who we areAkkodis is a global digital engineering and smart industry leader, bringing together talent and technology to engineer a smarter future. With more than 50,000 experts worldwide and over 1,000 in Belgium, we support companies across industries in innovation, digital transformation and R&D; from consulting and talent solutions to end-to-end project...