01.05.2024 | Full-time | PharmiwebParexel is in the business of improving the world’s health. We do this by providing a suite of biopharmaceutical services that help clients across the globe transform scientific discoveries into new treatments. From clinical trials to regulatory, consulting, and market access, our therapeutic
Uita-te mai târziu01.05.2024 | Full-time | PharmiwebCountries, Fortrea is transforming drug and device development for partners and patients across the globe. In this role you are accountable for performance and compliance for assigned protocols in a country in compliance with ICH/GCP and country regulations, Fortrea client’s policies and procedures, quality
Uita-te mai târziu01.05.2024 | Full-time | PharmiwebDescription Site Start-Up Regulatory Coordinator with Portuguese AND/OR Italian - single sponsor (FSP)/Site Contracts support Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs
Uita-te mai târziu01.05.2024 | Full-time | PfizerROLE SUMMARY Regulatory Quality Assurance (RQA) is an independent Quality audit function accountable to identify risks and non-compliance associated with Pfizer’s GxP regulated operations. Within RQA, the GMP Audit function is responsible for performing GMP audits to Pfizer facilities, contract
Uita-te mai târziu01.05.2024 | Full-time | PharmiwebParexel is in the business of improving the world’s health. We do this by providing a suite of biopharmaceutical services that help clients across the globe transform scientific discoveries into new treatments. From clinical trials to regulatory, consulting, and market access, our therapeutic
Uita-te mai târziu01.05.2024 | Full-time | PharmiwebCountries, Fortrea is transforming drug and device development for partners and patients across the globe. In this role you are accountable for performance and compliance for assigned protocols in a country in compliance with ICH/GCP and country regulations, Fortrea client’s policies and procedures, quality
Uita-te mai târziu01.05.2024 | Full-time | PharmiwebCountries, Fortrea is transforming drug and device development for partners and patients across the globe. In this role you are accountable for performance and compliance for assigned protocols in a country in compliance with ICH/GCP and country regulations, Fortrea client’s policies and procedures, quality
Uita-te mai târziu01.05.2024 | Full-time | PharmiwebOr remotely) ensuring regulatory, ICH-GCP and/or Good Pharmacoepidemiology Practice (GPP) and protocol compliance. Uses judgment and experience to evaluate overall performance
Uita-te mai târziu01.05.2024 | Full-time | Oradea | PharmiwebDescription Site Start-Up Regulatory Coordinator with Portuguese AND/OR Italian - single sponsor (FSP)/Site Contracts support Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs
Uita-te mai târziu01.05.2024 | Full-time | Signant HealthFor successful delivery of localisation activities, to meet key project milestones, whilst adhering to Good Clinical Practice (GCP), Signant Health processes and regulatory compliance. Prior knowledge of handling multi and complex tasks, on a volume of projects is seen as an asset/would be advantageous. Want
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