Management Jobs in Ghent

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Communications Manager - Internal Affairs

Michael Page

Gent

Because of organizational optimization they are looking for a Communications Manager - Internal Affairs for their head quarters. * Being the contact person between (corporate) project teams and local communication partners within the different regions. * Providing support for C-level communications. * You have at least five years of professional experience within corporate communication. * You are able to adapt your communication style according to your target audience. Michael Page * Ghent * Contract duration unspecified * Full Time - Our client is of synthetic materials. They are world renowned and compete with some of the largest names in the industry. In Europe they are number 2 within their activity. Manufacturing and Production, Chemicals, Gent, Lokeren, Antwerp - Your responsibilities * Communicating about strategic initiatives and programs within the company through different channels. Because of organizational optimization they are looking for a Communications Manager - Internal Affairs for their head quarters. * Being the contact person between (corporate) project teams and local communication partners within the different regions. * Providing support for C-level communications. * You have at least five years of professional experience within corporate communication. * You are able to adapt your communication style according to your target audience. Michael Page * Ghent * Contract duration unspecified * Full Time - Our client is of synthetic materials. They are world renowned and compete with some of the largest names in the industry. In Europe they are number 2 within their activity. Manufacturing and Production, Chemicals, Gent, Lokeren, Antwerp - Your responsibilities * Communicating about strategic initiatives and programs within the company through different channels.
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Administrative Officer

Invibes Advertsing

Gent

Invibes is looking for an Administrative Officer! We are looking for a positive & enthusiast Administrative Officer to join our Finance Department. Invibes Advertsing * Ghent * Contract duration unspecified * Full Time - You would be Quarters, only 2 minutes' walk from the train station in Ghent! * Gathering all the necessary documents * Keep record of all the new and existing clients records * Staying in close contact with our commercials * Calculating the amounts to invoice and draft the invoices * and follow up on over dues * Factoring management * Monthly bonus calculations for the commercial teams * You have a degree in administration or some years of relevant experience, preferably in an international environment * Some excellent knowledge of Word and Excel * Since you would be working throughout Europe, this job requires high French and English spoken skills as well as written skills Invibes is looking for an Administrative Officer! We are looking for a positive & enthusiast Administrative Officer to join our Finance Department. Invibes Advertsing * Ghent * Contract duration unspecified * Full Time - You would be Quarters, only 2 minutes' walk from the train station in Ghent! * Gathering all the necessary documents * Keep record of all the new and existing clients records * Staying in close contact with our commercials * Calculating the amounts to invoice and draft the invoices * and follow up on over dues * Factoring management * Monthly bonus calculations for the commercial teams * You have a degree in administration or some years of relevant experience, preferably in an international environment * Some excellent knowledge of Word and Excel * Since you would be working throughout Europe, this job requires high French and English spoken skills as well as written skills
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QA Manager GCP

Real Staffing Brussels (International)

Ghent

I am helping an international company based in Ghent to find their QA Manager for clinical processes (GCP). As GCP QA manager you will be responsible for the quality aspect of the clinical trials globally. Real Staffing Brussels (International) * Ghent * Contract duration unspecified * Full Time - Real Staffing - Your responsibilities * Lab activities for clinical research * Performing clinical trials for third parties - It's a growing organisation using cutting edge science in their HQ in Ghent. This implicates that all the decisions are made in Belgium and you will be on top of every change and always be up to date. This aspect gives good opportunities in the perspective of growth. You will work in a team of 4 professionals who are all responsible for their own processes in their specific field. Responsibilities * Define, describe and optimise the procedural framework for operational processes; I am helping an international company based in Ghent to find their QA Manager for clinical processes (GCP). As GCP QA manager you will be responsible for the quality aspect of the clinical trials globally. Real Staffing Brussels (International) * Ghent * Contract duration unspecified * Full Time - Real Staffing - Your responsibilities * Lab activities for clinical research * Performing clinical trials for third parties - It's a growing organisation using cutting edge science in their HQ in Ghent. This implicates that all the decisions are made in Belgium and you will be on top of every change and always be up to date. This aspect gives good opportunities in the perspective of growth. You will work in a team of 4 professionals who are all responsible for their own processes in their specific field. Responsibilities * Define, describe and optimise the procedural framework for operational processes;
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Agile Project Manager

Inetum-Realdolmen

Gent

As an Agile Project Manager organization, you ensure that the project goes forward, you identify and remove obstacles for the team. * Continuously developing yourself to keep up with the latest developments and trends within agile methodologies, project- & service delivery management and IT in general? You also monitor project and support risks and clean up blocking issues. You plan the necessary meetings with the client and reports regularly on the progress of project- and support contracts. Being a real team player, you know what is happening in the team and you help them to organize themselves agile. * You track the progress of the teams and you consult with the parties involved in the projects and support contracts * You pro-actively evaluate project and support risks and take the necessary measures. * A people manager with excellent communication and motivational skills? As an Agile Project Manager organization, you ensure that the project goes forward, you identify and remove obstacles for the team. * Continuously developing yourself to keep up with the latest developments and trends within agile methodologies, project- & service delivery management and IT in general? You also monitor project and support risks and clean up blocking issues. You plan the necessary meetings with the client and reports regularly on the progress of project- and support contracts. Being a real team player, you know what is happening in the team and you help them to organize themselves agile. * You track the progress of the teams and you consult with the parties involved in the projects and support contracts * You pro-actively evaluate project and support risks and take the necessary measures. * A people manager with excellent communication and motivational skills?
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Trial Set-Up Quality Manager

Real Staffing Brussels (International)

Ghent

Because of their growth, I am helping an international company, based in Ghent, to find their new Trial Set-up Quality Manager. where you will execute a quality review function, reporting to the Global Trial Set-Up lead. * Performing clinical trials for third parties - Global Trial Set-up Lead - You will be the last checkpoint before the information is released, processed, and communicated towards the Project Managers. * Quality review of documentation and database, internally and externally; o Trial Documents; o Local Trial Set-up * Quality Mindset ; * Knowledge of/or basics of clinical trials; experience in a CRO or Central Laboratory; Real Staffing Brussels (International) * Ghent * Contract duration unspecified * Full Time - Real Staffing - Your responsibilities * Central Lab activities for clinical research - It's a growing organisation using cutting edge science in their HQ in Ghent. Because of their growth, I am helping an international company, based in Ghent, to find their new Trial Set-up Quality Manager. where you will execute a quality review function, reporting to the Global Trial Set-Up lead. * Performing clinical trials for third parties - Global Trial Set-up Lead - You will be the last checkpoint before the information is released, processed, and communicated towards the Project Managers. * Quality review of documentation and database, internally and externally; o Trial Documents; o Local Trial Set-up * Quality Mindset ; * Knowledge of/or basics of clinical trials; experience in a CRO or Central Laboratory; Real Staffing Brussels (International) * Ghent * Contract duration unspecified * Full Time - Real Staffing - Your responsibilities * Central Lab activities for clinical research - It's a growing organisation using cutting edge science in their HQ in Ghent.
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GROUP CONSOLIDATION OFFICER | ENGLISH | PERMANENT CONTRACT

HAYS

Zaventem

For an international company located in Zaventem, HAYS Accounting is looking for a Group Consolidation Officer. As Consolidation officer, you . Are you the Group Consolidation Officer that we're looking? 3 y. experience in audit, consolidation or analytical bookkeeping - You are a strong support of the group accounting manual and procedures and the preparation of the consolidation process. You have a master's degree in finance (or in business administration) and you have at least 3 years' experience as auditor or in consolidation, within a large group and/or an international environment. * Zaventem * Contract duration unspecified * Full Time * English, a knowledge of French or Dutch is an asset * Min. * A Master degree is required * International company * Opportunity to grow within the company * Permanent contract - Your responsibilities - You support and collaborate with your management at group level. For an international company located in Zaventem, HAYS Accounting is looking for a Group Consolidation Officer. As Consolidation officer, you . Are you the Group Consolidation Officer that we're looking? 3 y. experience in audit, consolidation or analytical bookkeeping - You are a strong support of the group accounting manual and procedures and the preparation of the consolidation process. You have a master's degree in finance (or in business administration) and you have at least 3 years' experience as auditor or in consolidation, within a large group and/or an international environment. * Zaventem * Contract duration unspecified * Full Time * English, a knowledge of French or Dutch is an asset * Min. * A Master degree is required * International company * Opportunity to grow within the company * Permanent contract - Your responsibilities - You support and collaborate with your management at group level.
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Administrative Assistant

FAMI-QS

Brussels

The FAMI-QS Secretariat is currently seeking to hire a part-time Administrative Coordinator. * Minimum required working experience: 3 years of demonstrable experience providing administrative office management and communication support in a similar role. * Brussels * Contract duration unspecified * Home Office - Introduction - Part-Time Employment in an international environment as a member of a small dynamic team - FAMI-QS is a sector-specific conformity assessment scheme for the sector of Specialty Feed Ingredients and their Mixtures. The main focus of the role is to assist with the day-to-day operations of the organisation, provide support to ongoing and future projects and perform other duties and responsibilities based on the needs of the organisation. Job description - Responsabilities * Review/proofreading of documents in English and French * Assisting with the invoicing The FAMI-QS Secretariat is currently seeking to hire a part-time Administrative Coordinator. * Minimum required working experience: 3 years of demonstrable experience providing administrative office management and communication support in a similar role. * Brussels * Contract duration unspecified * Home Office - Introduction - Part-Time Employment in an international environment as a member of a small dynamic team - FAMI-QS is a sector-specific conformity assessment scheme for the sector of Specialty Feed Ingredients and their Mixtures. The main focus of the role is to assist with the day-to-day operations of the organisation, provide support to ongoing and future projects and perform other duties and responsibilities based on the needs of the organisation. Job description - Responsabilities * Review/proofreading of documents in English and French * Assisting with the invoicing
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Clinical Project Manager

Oxford Global Resources

Herzele

Under the direction of the Associate Director, Clinical Operations, the Clinical Project Manager has responsibility for the comprehensive . Do you have experience as a Clinical Project Manager or are you able to lead a team to success? The Clinical Project Manager may also participate in the development of SOPs, and internal monitoring processes. * Ability to execute and manage all aspects of multi-center global clinical trials independently from concept to close-out within designated project budgets and timelines * On assigned studies, provide leadership for the clinical operations project team, for the execution of all services according to the project-specific scope of work * A minimum of 2 years of clinical project management experience * Develop clear and measurable project management plans and establish project metrics Under the direction of the Associate Director, Clinical Operations, the Clinical Project Manager has responsibility for the comprehensive . Do you have experience as a Clinical Project Manager or are you able to lead a team to success? The Clinical Project Manager may also participate in the development of SOPs, and internal monitoring processes. * Ability to execute and manage all aspects of multi-center global clinical trials independently from concept to close-out within designated project budgets and timelines * On assigned studies, provide leadership for the clinical operations project team, for the execution of all services according to the project-specific scope of work * A minimum of 2 years of clinical project management experience * Develop clear and measurable project management plans and establish project metrics
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Data Manager

FERN VALLEY

East-Flanders

For the expansion of our client's clinical team, we are looking for a Clinical Data Manager (CDM). The CDM is responsible for all clinical data management aspects for the assigned global clinical studies from preparation until archiving. * Responsible for leading, guiding and overseeing the CROs data management activities and responsible for overseeing vendors involved in the assigned clinical studies based upon metrics and plan * contract negotiations together with the company's clinical study manager and Director Vendor Management * Providing input into and/or developing study related materials such as Clinical Study Protocol, Clinical Monitoring Plans, Data Management Plans, eCRF/EDC and Edit Check Specifications, eCRF completion guidelines, External Data Reconciliation Plans, SAS Listing Specifications, Lab Data Transfer Plans, etc. For the expansion of our client's clinical team, we are looking for a Clinical Data Manager (CDM). The CDM is responsible for all clinical data management aspects for the assigned global clinical studies from preparation until archiving. * Responsible for leading, guiding and overseeing the CROs data management activities and responsible for overseeing vendors involved in the assigned clinical studies based upon metrics and plan * contract negotiations together with the company's clinical study manager and Director Vendor Management * Providing input into and/or developing study related materials such as Clinical Study Protocol, Clinical Monitoring Plans, Data Management Plans, eCRF/EDC and Edit Check Specifications, eCRF completion guidelines, External Data Reconciliation Plans, SAS Listing Specifications, Lab Data Transfer Plans, etc.
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