Clinical Regulatory Affairs Specialist

**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...

**Solliciteren tot en met: 09-04-2024**: **Verleg grenzen binnen het Clinical Trial Center (CTC)**: Het Clinical Trial Center (CTC) staat in voor de administratieve coördinatie van klinische onderzoeksactiviteiten binnen UZ/KU Leuven. Als kenniscentrum voor klinische studies biedt het CTC integrale ondersteuning aan alle medisch en paramedisch...

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...

**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...

**Solliciteren tot en met: **:**Verleg grenzen binnen het Clinical Trial Center (CTC)**:Het Clinical Trial Center (CTC) staat in voor de administratieve coördinatie van klinische onderzoeksactiviteiten binnen UZ/KU Leuven. Als kenniscentrum voor klinische studies biedt het CTC integrale ondersteuning aan alle medisch en paramedisch wetenschappelijk...

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 dental...

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...

Seniority Level: AB InBev is seeking a Science and Regulatory Affairs (SRA) Specialist for our Global SRA team in the Global Innovation & Technology Center (GITEC), in Belgium. At the heart of our dynamic global growth is a simple belief: nothing should come between incredibly talented people and an accelerated career. That is why we dream big. Why we look...

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...

Seniority Level:AB InBev is seeking a Science and Regulatory Affairs (SRA) Specialist for our Global SRA team in the Global Innovation & Technology Center (GITEC), in Belgium.At the heart of our dynamic global growth is a simple belief: nothing should come between incredibly talented people and an accelerated career. That is why we dream big. Why we look to...

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...

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...

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 study...

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...

**We are looking for a Clinical Data Coordinator for our client in the health sector based in Leuven.** **Job description**: **Responsibilities**: - Create and manage clinical trial databases, including data entry and quality control checks - Work with clinical research staff to collect and organize study data - Generate study reports and ensure accuracy...

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: Our clinical operations activities are growing rapidly and we are currently seeking full-time, Regulatory Submissions Technical Advisor to join our Site Activation and Maintenance team, within Clinical Operations in Leuven, Belgium. This position plays a key role at Medpace, preparing and reviewing regulatory documents and providing strategic...

Job Summary: Our clinical operations activities are growing rapidly and we are currently seeking full-time, Regulatory Submissions Technical Advisor to join our Site Activation and Maintenance team, within Clinical Operations in Leuven, Belgium.This position plays a key role at Medpace, preparing and reviewing regulatory documents and providing strategic...

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 use...

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...