Regulatory Submissions Coordinator

My Client who is a very successful, mid-size CRO are currently looking for a Regulatory Submission Manager to join their team in Leuven (Belgium). They are constantly growing, which allows for your personal growth as well as great opportunities to develop & grow your career. Along with that you will receive top quality training which has been voted one of...

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...

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 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...

Company Description PSI is a leading Contract Research Organization with more than 27 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. **Job Description**: Join our team of experts in regulatory...

An international medical device/pharma company is looking for an RA Associate to join the team with a RA Manager, Senior RA Manager and a RA Director. This is a small team where you will be involved in all the Regulatory Affairs activities worldwide meaning you will have a lot more variety and will be able to learn something new every day. It is a small...

Company Description We are the company that cares - for our staff, for our clients, for our partners and for the quality of work we do. A dynamic, global company founded in 1995, we bring together more than 1,700 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those who...

Company Description We are the company that cares - for our staff, for our clients, for our partners and for the quality of work we do. A dynamic, global company founded in 1995, we bring together more than 1,700 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those who...

Company Description We are the company that cares - for our staff, for our clients, for our partners and for the quality of work we do. A dynamic, global company founded in 1995, we bring together more than 1,700 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those who...

Oliver James is looking for **_a KYC Coordinator for one of the most important bank in Europe. _**Do you already have some experience as AML analyst or KYC and you dream of being part of one of the largest banks in the country? Then, the person we want is you! **_ Role Purpose_** *** The Analyst is responsible for conducting an onboarding review in line...

Job Summary: Our clinical activities are growing rapidly, and we are currently seeking a full-time Regulatory Submissions Coordinator 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 your previous expertise...

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...

Comate is looking for a motivated **Quality Assurance and Regulatory Affairs (QA/RA) engineer **to support its growth and expansion in the **Life Sciences** sector. The aim of our passionate team is to cooperate with our clients in order to develop a unique product that is more innovative and more advanced than anything that is currently available on the...

Clinical Data Coordinator | Full-time | CDI | English | Leuven | 1094058 Hays is looking for a Clinical Data Coordinator Lab to join our client data management team. **Your responsibilities as a Clinical Data Coordinator Lab** In this role, you will have the opportunity to play a crucial part in ensuring the accuracy and completeness of our data by...

An international medical device/pharma company is looking for an RA Manager to join the RA team and will work closely together with QA and R&D. The Regulatory Affairs activities worldwide are coordinated by the Belgian office as well for the pharmaceutical as medical device submissions meaning you will have a better helicopter view and will have a bigger...

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...

Job Summary: Our imaging services are growing rapidly, and we are currently seeking a full-time **Imaging Project Coordinator**to join our team in Leuven. 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: - Review incoming medical...

**Wat ga je doen?**: For our partner, an international player in Laser production, we are looking for a CE certification coordinator. The responsibilities of the futur colleague: Develop and implement CE local certification of the machines, ensure compliance with local regulations. Conduct regular safety inspections and audits for CE local certification of...

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...

Job Summary: Our corporate activities are growing rapidly, and we are currently seeking a full-time Data Coordinator to join our Core Laboratory/Imaging Services 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 your previous expertise and...