03.06.2024 | Full-time | PharmiwebIn accordance with regulatory requirements, i.e., Good Clinical Practice and International Conference on Harmonization guidelines Managing progress by tracking regulatory submissions, recruitment, case report form completion, and data query resolutions Collaborating with experts at study sites and with client
Uita-te mai târziu03.06.2024 | Full-time | Cluj-Napoca | 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 târziu03.06.2024 | Full-time | PharmiwebIn Romania . Responsibilities include All details of site management as prescribed in the project plans Recruitment of potential investigators, preparation of EC submissions, notifications to regulatory authorities, translation of study-related documentation, organization of meetings and other tasks
Uita-te mai târziu03.06.2024 | Full-time | PharmiwebIn Romania . Responsibilities include All details of site management as prescribed in the project plans Recruitment of potential investigators, preparation of EC submissions, notifications to regulatory authorities, translation of study-related documentation, organization of meetings and other tasks
Uita-te mai târziu03.06.2024 | Full-time | HCLTechIn Exchange Online, Microsoft 365 eco system, sharepoint migration" (1.) To provide support for on call escalations and doing root cause analysis of given issue (2.) To independently resolve tickets within agreed SLA of ticket volume and time (3.) To adhere to quality standards, regulatory requirements
Uita-te mai târziu03.06.2024 | 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 târziu03.06.2024 | 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 târziu03.06.2024 | Full-time | PharmiwebFor clinical studies across various phases, ensuring adherence to applicable regulations and principles of ICH-GCP. Responsibilities Travel to sites to carry out site selection, initiation, monitoring and close-outs. Support the development of a subject recruitment plan. Evaluate the quality and integrity
Uita-te mai târziu03.06.2024 | Full-time | Cluj-Napoca | 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 târziu03.06.2024 | 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
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