Vacatures Clinical medical affairs Gent

 ...Head of Regulatory Affairs EMEA page is loaded Head of Regulatory Affairs EMEA Apply...  ...regulatory approvals, trends, and dynamics in clinical areas of interest to the company, and...  ...and materials review Partner with medical, legal, quality, PV, market access and distribution... 

 ...As we are growing, we are currently looking for a Clinical Trial Manager (CTM). The CTM is responsible for all operational aspects...  ...systems, eCRF databases) Bachelor’s degree or University degree – medical or para-medical (Biology, Biomedical Sciences, Pharmacy,... 

 ...processing & retail, the professional cleaning industry, and the medical and life sciences sectors. Rapid company growth and an...  ...environment in Europe raises the need to strengthen our Regulatory Affairs Department. Christeyns is looking for a (M/F/D) Director Regulatory... 

 ...Enterprise Imaging Platform is purpose-built to reduce complexity, improve productivity and deliver clinical value. We use our proven track record as an innovator, our in-depth medical knowledge and our strategic guidance to help healthcare providers achieve their clinical,... 

 ...Jordan Griffiths is managing a CRO client that requires a Project Manager/Operations Manager position. The role combines 60% Clinical Project Manager and 40% Operations Management responsibilities. Responsibilities: Bear full responsibility for managing clinical... 

 ...QA Officer - Medical Devices Opportunity in Gent, Belgium This company is a small MedTech company of approximately 60 people, fostering in-depth relationships among colleagues and maintaining a flat hierarchy system internally. The organisation is a trailblazer in the... 

 ...in Scientific background: Master or PhD, in Chemistry, Biochemistry, Toxicology. ~3 to 5 of industry experience within Regulatory Affairs (registration, development, maintenance). ~ Experienced in Chemical Legislation, Chemical industry, Chemical Regulations (i.e.... 

 ...As a Senior Regulatory Affairs Specialist, you will be responsible for ensuring compliance with regulatory requirements for biocide products. You will work closely with cross-functional teams, regulatory authorities, and external partners to facilitate the registration... 

 ...Medical Information Senior Manager – Content Management page is loaded Medical Information Senior Manager – Content Management Apply...  ...and accurate responses are provided to unsolicited medical and clinical inquiries from healthcare professionals, patients, clinical... 

 ...Our client is an American Biomedical company that specializes in researching blood samples. With this research they try to develop medication for patients with long-term and chronic diseases. Since a few years the company is also located in Belgium, in Ghent. Through... 

Cette page a été éditée automatiquement par un moteur de traduction. Toutes nos excuses pour les éventuelles fautes de frappe ! Support technique qualité - Dispositifs médicaux Vous travaillerez dans une organisation plus petite, avec des lignes de décision courtes...

 ...voorbereiding en het indienen van nationale dossiers in het kader van de Biocidal Products Regulation. Je rapporteert aan de Regulatory Affairs Director op het hoofdkwartier te Gent. Wie ben jij? m/v/x ~ Het is zeer belangrijk dat deze persoon nauwkeurig en precies kan... 

Onze klant werd opgericht in 1889 en is een internationaal concern in medische apparatuur en veiligheidstechniek. Wereldwijd tellen ze meer dan 16.000 werknemers is het vertegenwoordigd in meer dan 190 landen en in meer dan 50 landen met een eigen sales- en serviceorganisatie...

 ...always wanted to work for one of the world's best employers within medical technology and an award-winning Great Place to Work Belgium?...  ...innovative Mako robotics system, we are looking for a Hybrid Clinical (Mako) Support Specialist to cover the regions of Oost- en... 

 ...in more than 100 markets around the world. In order to sustain their growth in EU, they are looking to extend their regulatory affairs team and add a strong team player to drive change & project internally & externally. Job Description As the successful Regulatory... 

 ...Post-doctoral assistant Department of Basic and Applied Medical Sciences (27062) { const baseUrl = $event.detail.baseUrl; const currentUrl...  ...and master level) You are responsible for the course on clinical pharmacology at the master of Science in Nursing and Midwifery... 

 ...bringing their valuable molecules to the clinic and market. Our commitment extends to providing...  ...with experts to innovate drugs for unmet medical needs, Ardena could be the ideal...  ...experience in the dynamic field of regulatory affairs. YOUR KEY RESPONSIBILITIES Write... 

Our client, a private clinic located in East-Flanders, specialises in a range of eye care services. The clinic has a team of experienced...  ...country Have an EU/EEA citizenship Hold an EU/EEA medical or a specialist diploma Master English (or French) in a full... 

 ...immunogenicity assay development/validation for large molecules and/or clinical immunogenicity risk assessment and data interpretation....  ...Protocol, Data Transfer Agreement, lab manual). • Work closely with Medical Writers to draft bioanalytical modules and immunogenicity... 

 ...consists of 2 independent laboratories: Labo Nuytinck, active in medical analytics and AnaBioTec, active in drug development. Both labs...  ...as well as established pharma companies worldwide from pre-clinical drug characterization and assay development, through clinical phases...