Study Start Up, Regulatory Submissions Coordinator

55000 EUR - 55000 EUR - Leuven - Belgium, Belgium - Permanent Study Start Up & Regulatory Coordinator - Global CRO - Belgium I am currently working alongside my client, a global CRO with a long and rich history within Clinical Research, to support them in their search for a Study Start Up & Regulatory Submissions Coordinator to join their growing...

55000 EUR EUR Leuven Belgium, Belgium PermanentStudy Start Up & Regulatory Coordinator - Global CRO - BelgiumI am currently working alongside my client, a global CRO with a long and rich history within Clinical Research, to support them in their search for a Study Start Up & Regulatory Submissions Coordinator to join their growing organisation and their...

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 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 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...

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...

Job Summary: Our clinical operations activities are growing rapidly, and we are currently seeking a full-time Regulatory Submissions Manager to join our Clinical Operations team in Leuven, Belgium. This position plays a key role in the clinical trial management process at Medpace. If you want an exciting career where you use your previous expertise and can...

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 a full-time Regulatory Submissions Manager to join our Clinical Operations team in Leuven, Belgium. This position plays a key role in the clinical trial management process at Medpace. If you want an exciting career where you use your previous expertise and can...

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...

**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 operations activities are growing rapidly, and we are currently seeking a full-time Regulatory Submissions Manager to join our Clinical Operations team in Leuven, Belgium. This position plays a key role in the clinical trial management process at Medpace. If you want an exciting career where you use your previous expertise and can...

Clinical Data Coordinator | Full-time | CDI | English | Leuven | 1094059 Hays is looking for a Clinical Data Coordinator (CRO) to join our client data management team. **Your responsibilities as a Clinical Data Coordinator (CRO)** In this role, you will have the opportunity to put your analytical skills to use by validating database designs, reporting on...

Job Summary: Our corporate activities are growing rapidly, and we are currently seeking a full-time, office-based **eClinical Coordinator** to join our Data Management team. By working with the eClinical Project Manager and other team members, these professionals ensure the accuracy of data that is reported by patients for clinical studies. If you are...

Job Summary: Our clinical activities are growing rapidly, and we are currently seeking a full-time Site Relationship Coordinator to join our vibrant Clinical Operations team. This is a fantastic opportunity to work on pre-award and post-award study feasibilities, build and maintain strategic relationships with our network of sites, and develop key strategies...

Job Summary: Our clinical activities are growing rapidly, and we are currently seeking a full-time Site Relationship Coordinator to join our vibrant Clinical Operations team. This is a fantastic opportunity to work on pre-award and post-award study feasibilities, build and maintain strategic relationships with our network of sites, and develop key strategies...

Competitive Leuven, Belgium PermanentProject Coordinator - Belgium - Mid-Sized CRO - Fast Career ProgressionThis established organisation is a Mid-Sized CRO that has been around for over 30 years. It is one of the leading CROs for BioTech Sponsors which contrasts with the typical Pharma-heavy CROs. They provide a modern and dynamic working environmentThis...

Job Summary: We are currently seeking a full-time Imaging Project Coordinator to join our team. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you. Responsibilities: - Compile and maintain project-specific status reports and project timelines...

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...

Hobson Prior is in search of a dedicated individual for the position of Medical Safety Operations. This role is centered around ensuring compliance with pharmacovigilance operational processes in assigned projects and collaborating with external service providers. The chosen candidate will play a key role in organizing the development of study-specific...