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83 resultaten voor Clinical monitor in Asse binnen een straal van 30 km
Als clinical research associate hou jij het overzicht over onze studies.
We hebben je zoekopdracht uitgebreid met 82 gelijkaardige vacatures.
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Monitor and trend vendor performance * Work closely with in the Corporate QA teams (especially CM&C Clinical Supply QA, Corporate Compliance and Affiliate Quality Services) and key Technical Operations teams/Affiliate teams to ensure that all QA services for selected critical vendors are provided in an effective and efficient way - Operational GMP experience or clinical activities experience would be a distinct advantage.
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Snel solliciteren
SGS Life Sciences carries out all type of services for pharmaceutical and biotechnology companies, from coordination and running of clinical trials with new molecules or techniques on human beings, to support and consultancy on post marketing registration activities. * Manage and monitor all installed systems, infrastructure, and application deployments on Azure Cloud.
Drive and promote a continuous quality and compliance mindset within Clinical Packaging & Logistics Operations, ensuring compliance with cGMP's and the company Quality Management System * Partner with Clinical Supply Compliance Team and management to quality initiatives that develop and maintain a high performing, scalable, and compliant quality system in CPLO. * Distribute daily team work, monitor actual vs. theoretical throughput rates.
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As an Orthodontic Clinical Advisor – Dental Solutions (m/f/*) reporting to the Benelux Sales Leader, you will have the opportunity to tap into your curiosity and collaborate with some of the most innovative and diverse people around the world. * Co-traveling with sales reps and providing clinical and technical information that supports and enhances the sales presentation. * Experience in Orthodontic Clinical Advisor role
Snel solliciteren
SGS Pharma Clinical Research carries out all type of services for pharmaceutical and biotechnology companies, from coordination and running of clinical trials with new molecules or techniques on human beings, to full-service support and consultancy throughout the clinical development process. We currently have a unique opportunity for a Global Director Business Development for Clinical Research - The Global Director Business Development (GBDM) provides leadership and coaching to the Business Development Managers and is responsible for the management of all business development activities of SGS Clinical Research, identifying and exploring strategic business development opportunities to maximize organization growth. * be accountable for the target realization of the sales and business
In the spirit of continued growth, we are currently looking for a Head Clinical Project Management. As Head Clinical Project Management (HCPM) you will provide leadership to the team of Clinical Project Managers (CPM) and ensure the allocation of the appropriate CPM resource to the projects. You will work in close collaboration with the CO, Operational Manager Clinical Operations and Clinical Project Manager Coordinator to evaluate resource and training needs of the team. As HCPM, you may assume the responsibilities of a Project Manager in the management of clinical research projects. * Line management: managing and coaching the clinical project management team, providing them with support, advice and assistance, evaluating their training needs, organ
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Monitor HR Consulting - Voor meer informatie kan je terecht bij Monitor HR Consulting. Monitor HR ConsultingBevrijdingslaan 201, 9200 Dendermonde, België
Monitor HR Consulting - Voor meer informatie kan je terecht bij Monitor HR Consulting. Monitor HR ConsultingIkaroslaan 6, 1930 Zaventem, België
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Le Clinical Trial Center (CTC) de l'H.U.B est une unité centralisée de gestion de la recherche.
Snel solliciteren
SGS Life Sciences carries out all type of services for pharmaceutical and biotechnology companies, from coordination and running of clinical trials with new molecules or techniques on human beings, to support and consultancy on post marketing registration activities. You support the Business Development and Procurement team in the set-up and review of clinical research related agreements (master service agreements, stand-alone service agreements and work orders). Content wise you get help from the departments concerned to set-up and review the clinical research related agreements. General understanding of clinical development / contracting is of course a big plus!
Snel solliciteren
As Business Development Manager you will be responsible for identifying and exploring strategic business development opportunities within the Clinical Research business to maximize organization growth. * that with your extensive knowledge of current market evolutions and conditions you will be responsible for the growth of our Clinical research Business with both new and existing customers, with an emphasis on customer satisfaction and repeat business; * You have experience within the fields of Clinical research and CRO business, or other associated, relevant businesses. * The clinical drug development process has no secrets for you.
Snel solliciteren
As Business Development Manager you will be responsible for identifying and exploring strategic business development opportunities with a focus on biometrics activities within the Clinical Research business to maximize organization growth. * You have experience within the fields of Clinical research and CRO business, solid technical understanding of the biometrics (data management and/or biostatistics) space, or other associated, relevant businesses. * The clinical drug development process has no secrets for you.
The primary responsibility of the Global is the organization and coordination of site feasibilities for all multicenter Phase II-IV clinical trial projects. * A basic to intermediate understanding of clinical trials and key elements of a trial protocol. * At least 1 year of experience in clinical trial conduct or management (phase I-III) at the site, CRO, or sponsor level would be preferred.
Snel solliciteren
SGS Life Sciences carries out all type of services for pharmaceutical and biotechnology companies, from coordination and running of clinical trials with new molecules or techniques on human beings, to support and consultancy on post marketing registration activities. * Reviewing and/or providing input in the study protocol (sample size calculations), CRF and clinical study report * You want to work in a young and dynamic group of clinical programmers and statisticians
Snel solliciteren
As a Key Account Manager, you will focus on a select number of identified key/strategic clients and work to embed and grow business opportunity from a global SGS Clinical Research perspective. You will act as the point of contact between the client and the SGS Clinical Research Organization. * You have experience within the fields of Clinical Research and CRO business, or any other associated, relevant business.
Snel solliciteren
SGS Life Sciences carries out all type of services for pharmaceutical and biotechnology companies, from coordination and running of clinical trials with new molecules or techniques on human beings, to support and consultancy on post marketing registration activities. * Implementation of CDISC standards in clinical trials * Quality control of project deliverables * You want to work in a young and dynamic group of clinical programmers and statisticians
As a Gene Therapy Quality Partner, you will support the Genesis project GMP Readiness program to timely obtain health authorities authorization to manufacture Gene Therapy clinical batches in the new facility pilot plant.
Work closely with Clinical Manufacturing Teams to ensure that the Quality Management System in support of product development and clinical supplies, work in a way that ensure product quality, safety and efficacy, meet regulatory requirements and expectations and operate in a fit for purpose and in a smarter way. * More specifically, provide quality support for qualification and validation activities related to Clinical Manufacturing activities like facilities cleaning processes, viable and non-viable environmental monitoring, equipment and system qualification/validation
Drive continuous quality improvement process, ensuring that the Quality Management System in support of product development and clinical supplies, work in a way that ensure product quality, safety and efficacy, meet regulatory requirements and expectations and operate in a fit for purpose and in a smarter way.
Le Clinical Trials Center (CTC) de l'H.U.B est un service de soutien, prenant en compte les aspects de la recherche clinique commerciale et académique, dont la mission est de fournir une assistance professionnelle à la recherche clinique en centralisant et en harmonisant la gestion administrative, opérationnelle, contractuelle et financière des études cliniques.
Als clinical trial assistant ben jij de administratieve spil van de studies.
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(Senior) Policy Advisor European Affairs
(Senior) Policy Advisor European Affairs
Gesamtverband der Deutschen Versicherungswirtschaft e.V.
Brussels
Monitor and analyze political and regulatory developments affecting the insurance industry
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Monitor and analyze market trends, competitive landscape, and customer needs to inform product strategy. * Monitor and control expenditures to stay within budget while maximizing product value.
Monitor and manage the documentation schedule.