03/06/2024 | Fulltime | | United Kingdom | CV-Library | €13 / Hour Will be responsible for ensuring the integrity of clinical trial supplies packaged at the site. Day to day duties include - Generating clinical trial packaging documentation to meet the company, Client, Study and Regulatory requirements. - Completing documentation in accordance to relevant SOPs and to comply
Save for later31/05/2024 | Fulltime | | United Kingdom | CV-Library | €30,000 - €41,000 / Year Electronics Engineer -Electronics Control Device and Sensor Development NuTissu are developing a Medical Device to address chronic wounds. The company is aiming to achieve rapid progress of a device development objectives to reach pre-clinical trials with the support of an exceptionally talented
Save for later31/05/2024 | Fulltime | | United Kingdom | CV-LibraryBank holidays Company Bonus – We do our best work to succeed together. When we achieve our goals you'll be rewarded through our bonus scheme Private Medical Cover – This gives you peace of mind, you have choice, flexibility and speed of access to the most clinically appropriate care via Bupa Pension
Save for later31/05/2024 | Fulltime | | United Kingdom | CV-Library | €26 / Hour And follow-up of all adverse event reports for all products from Clinical Trials, Non-interventional Studies, Patient Oriented Program (POPs), Literature, Spontaneous Reports, and any other source of information. Transcribe, translate, and enter data from source documents into safety systems accurately
Save for later30/05/2024 | Fulltime | | United Kingdom | CV-Library | €24,000 - €30,000 / Year The Personal Injury and Clinical Negligence department. Location St Helens As a Paralegal, you will be responsible for supporting the legal team in all aspects of case preparation and document management within Personal Injury and Clinical Negligence and Litigation. You will work closely with attorneys
Save for later30/05/2024 | Fulltime | | United Kingdom | CV-Library | €500 - €800 And operate effectively in accordance with UK, EU, regulatory requirements. Duties and Responsibilities - Carrying out the duties of a Qualified Person as defined in the Human regulations 2012 and Medicines for Human Use (Clinical Trials) regulation 2004 and EU guide to cGMP. - Releasing batches according
Save for later30/05/2024 | Fulltime | | United Kingdom | CV-Library | €140,000 - €150,000 / Year Of neuromodulation device design and/or complex implantable medical devices and risk management having worked under 13485 (or equivalent). Evidence of your team management and/or project leadership experience. Recent and relevant experience lead the engineering of a novel AIMD from development through to clinical
Save for later30/05/2024 | Fulltime | | United Kingdom | CV-LibraryEncompasses education, residential care and the clinical team To monitor progress and targets to ensure that each individual student can achieve planned outcomes Essential criteria Relevant experience of teaching pupils and young people with Autistic spectrum condition and/or challenging behaviours Relevant
Save for later29/05/2024 | Fulltime | | United Kingdom | CV-Library | €35,000 - €47,000 / Year Working in clinical research environment. Clinical skills such as phlebotomy, cannulation, taking ECGs. Knowledge of the clinical trial process Knowledge of ICH-GCP Highly effective communication skills Good organisational skills Good written and analytical skills Able to manage work autonomously
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