Study Start Up, Regulatory Submissions Coordinator

Job Summary: Our clinical activities are growing rapidly, and we are currently seeking a full-time Regulatory Submissions Coordinator (Study Start Up Specialist) to join our Clinical Operations team. This position will work on a team to accomplish tasks and projects that are instrumental to the company’s success. If you want an exciting career where you...

Job Summary: Medpace Reference Laboratories is a global, full-service central clinical trial laboratory specializing in a multitude of therapeutic areas. Our headquarters are located in Cincinnati, Ohio, USA and we are active in over 80 countries across the globe. Medpace has established laboratories in the USA, Europe, Singapore, and China. Our services...

We are currently seeking a **Lead Clinical Studies and Logistics** to join our “Clinical Development and Regulatory Affairs” team. As our Lead Clinical Studies and Logistics, you will be responsible for planning, executing, maintaining oversight and report on clinical trials, from planning, vendor selection (if applicable) and site feasibility, through...

Job Summary: Medpace Reference Laboratories is a global, full-service central clinical trial laboratory specializing in a multitude of therapeutic areas. Our headquarters are located in Cincinnati, Ohio, USA and we are active in over 80 countries across the globe. Medpace has established laboratories in the USA, Europe, Singapore, and China. Our services...

**GC Europe NV** is the European subsidiary of **GC Corporation**, a family-owned company with headquarters in Tokyo. It is one of the biggest suppliers of dental products with over 2300 employees all over the world and 4 production branches in Japan, the USA, China and Europe. We supply an entire range of consumer materials, equipment and facilities for...

At Terumo, we enhance lifesaving medical technologies for the benefit of society. Are you eager to contribute to people's health and patients' wellbeing? We'll challenge you to become a master in your field of expertise. You can invest your talents in balance with your personal aspirations - live and work in harmony. Built on our Japanese origins; we are...

Overview Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We...

Job Summary: Responsibilities: - Communicate and collaborate on global study activities; working closely with the project coordinator and clinical trial manager - Ensure timely delivery of recurrent tasks consistently with a high degree of accuracy - Compile and maintain project-specific status reports within the clinical trial management system - Interact...

The Director Assay Development leads an international and multidisciplinary team of scientists and lab technicians who have their main focus on developing a completely new molecular diagnostics device to be used at the point of need. He/she operates at the intersection between two major disciplines: silicon chip (biosensor) technologies and biochemistry. In...

Een innovatief **softwarebedrijf** en** start-up,** gevestigd in **Leuven** en gespecialiseerd in **enterprise performance management**, is momenteel op zoek naar een **ICT Business Consultant **vanwege hun indrukwekkende groei. Oorspronkelijk opgericht in **Nederland**, hebben ze hun invloed nu uitgebreid naar **Dubai **en **België**. Wat maakt deze kans...

At Terumo, we enhance lifesaving medical technologies for the benefit of society. Are you eager to contribute to people's health and patients' wellbeing? We'll challenge you to become a master in your field of expertise. You can invest your talents in balance with your personal aspirations - live and work in harmony. Built on our Japanese origins; we are...

Job Summary: Responsibilities: - Communicate and collaborate on global study activities; working closely with the project coordinator and clinical trial manager - Ensure timely delivery of recurrent tasks consistently with a high degree of accuracy - Compile and maintain project-specific status reports within the clinical trial management system - Interact...

Job Summary: Responsibilities: - Communicate and collaborate on global study activities; working closely with the project coordinator and clinical trial manager - Ensure timely delivery of recurrent tasks consistently with a high degree of accuracy - Compile and maintain project-specific status reports within the clinical trial management system - Interact...

Job Summary: We are seeking a full-time, office-based Fleet Coordinator to join our team in Leuven within a permanent contract. If you want an exciting career where you use your previous expertise in Facilities and have a strong desire to develop and grow your career even further, then this is the opportunity for you. Responsibilities: - The Fleet...

**GC Europe NV** is the European subsidiary of **GC Corporation**, a family-owned company with headquarters in Tokyo. It is one of the biggest suppliers of dental products with over 2300 employees all over the world and 4 production branches in Japan, the USA, China and Europe. We supply an entire range of consumer materials, equipment and facilities for...

Job Summary: Our corporate activities are growing rapidly, and we are currently seeking a full-time, office-based Data Coordinator for our Medpace Reference Laboratories to join our Data Management team in Leuven, Belgium. This position will work in a team to accomplish tasks and projects that are instrumental to the company’s success. By analysing...

**The **Opportunity**: Avantor is currently looking for someone with a Life Sciences or Legal (Bachelor/Professional Bachelor) to join our team as a Regulatory Affairs Officer on a fixed term contract until February 2025. This is a great opportunity for someone who wants to have a broad first experience within Regulatory Affairs within the Life Sciences...

**Start Date**: Mid/End November **FTE**: 0.2 **Location**: Belgium **Job Purpose** The Clinical Enrolment Manager (CEM) will perform site optimisation services in order to boost patient recruitment for clients’ clinical trials. The site optimisation services include, but are not limited to: Site Optimisation Calls - the telephone-based coaching of...

At Terumo, we enhance lifesaving medical technologies for the benefit of society. Are you eager to contribute to people's health and patients' wellbeing? We'll challenge you to become a master in your field of expertise. You can invest your talents in balance with your personal aspirations - live and work in harmony. Built on our Japanese origins; we are...

**Company Description** PSI is a leading Contract Research Organization with more than 25 years in the industry, offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications. PSI **Medical Monitors **provide medical input to global...