Clinical Affairs Officer (MedTech)
Who we are?
COVARTIM is an engineering company. Our mission is to help the MedTech industry foster medical innovation and improve health care.
More concrete we support any kind of organisation (practitioners, startups, SMEs, big companies) in the development and the certification of their medical technologies.
In a nutshell:
Launched in 2016 by Kyun, Founder and Director, passionate about medical technologies and working in the field for more than 15 years;
A (small) team of 15 people (24-52 years old) always ready to help each other (and play table football);
6 managers leading the team but also working on the projects: Emilie, Aurore, Eléonore, Arnaud, Laurent and Kyun;
40+ projects in parallel every month;
100+ clients in BeNeLux, France, USA, Japan, Finland, …
In order to answer the constantly growing demand from current and future clients, we are looking for a Clinical Affairs Officer.
The job is located in Brussels or in Liège for an open-ended period, to be filled immediately.
Practically, what will you do?
Prepare and manage submission for clinical investigations in EU and US;
Prepare CEP and CER;
Perform state of the art research and analysis;
Set up and follow up PMS, PMCF, PSUR;
Review and prepare documentation packages for notified bodies, FDA, competent authorities.
What about the team ?
Our members are gathered in two teams : the Development team and the Quality Assurance & Regulatory Affairs (QA/RA) team. As a Clinical Affairs Officer, you will join the QA/RA team that includes 6 people and that is led by Aurore.
The mission of the QA/RA team is to help our clients achieve the compliance of their devices with regards to the regulatory framework and to provide support for the introduction on the market.
Examples of projects:
Management of clinical investigation submission for a wearable diagnostic device (Class IIb);
Management of clinical investigation submission for a xenograft scaffold (Class III);
Review and update of CEP/CER for endoscopic tools (Class IIa, IIb);
Update of CEP/CER of IVD systems, including reagents (Class C).
In order to fulfill your mission, you will need:
A good understanding of Medical Devices and IVD regulatory environment (directives, regulations);
A good knowledge of medical devices clinical investigation clearance process (EU and US);
A good knowledge of medical devices risk management, CIP, CIR, CEP, CER, PMS, PMCF, PSUR;
A solid scientific background;
A good knowledge of literature search review;
To speak English and French/Dutch to communicate with our clients and our cosmopolitan team;
To make clients’ satisfaction a priority by combining quality and professionalism.
Every profile (seniority) is welcome!
You start your career? Our team will be there to guide you! You will collaborate on several projects and you will quickly have an overview of what can be done here. Cherry on top: you will learn and discover a lot in a short time!
You have got a first experience already? We will support you in the development and the enhancement of your knowledge and know-how. You will become more and more autonomous, take the lead on your projects and coordinate team work.
You have got a proven experience? We will be happy to make our clients and colleagues benefit from your expertise! You will get introduced to our methods then you will take the full lead on challenging projects.
Visit our website to learn more about our activities, our approach and our recruitment process.
Send your application today! We are looking forward to discuss your career in MedTech!