13.05.2024 | Full-time | PSIJob DescriptionThe Milestone One Site Coordinator role supports Clinical Study Sites in clinical trial related activities according to ICH-GCP, local regulations, protocol requirements within Study specific defined timelines and enrollment function of the role may include, but not limited
Uita-te mai târziu13.05.2024 | Full-time | StripeOf merchants, marketplaces, financial institutions and government regulators. Our new product distills the complex rules of tax into a platform with streamlined experiences that make tax filings easy and accurate. We are also one of the top emerging SaaS product offerings within Stripe and are enabling
Uita-te mai târziu13.05.2024 | 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 târziu13.05.2024 | Full-time | STRABAG s.r.l.Aufgaben Assist senior rail engineers in the tender and execution stages of railway infrastructure st in the review of project requirements, technical specifications, and regulatory standards to ensure compliance and aborate with project teams to coordinate construction
Uita-te mai târziu13.05.2024 | Full-time | Premier ResearchIn SAS programming within the area of clinical r experience using computerized information systems ledge of ICH and local regulatory authority
Uita-te mai târziu13.05.2024 | Full-time | IQVIAOr externallyMay mentor junior colleagues and engage in department knowledge sharingMay perform additional tasks as deemed appropriate by Line ManagerREQUIRED KNOWLEDGE, SKILLS AND ABILITIES Good understanding of the regulations, directives and guidance supporting clinical Research and DevelopmentDemonstrates
Uita-te mai târziu13.05.2024 | Full-time | OrganonAnd recommendations for aborating with sales, marketing, medical, regulatory, legal & compliance teams to ensure alignment and compliance of trade
Uita-te mai târziu13.05.2024 | Full-time | Signant HealthOf 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 to join the Best Team
Uita-te mai târziu13.05.2024 | Full-time | IQVIAClinical operation functions - monitoring, project and trial management, centralized support…- Data Sciences - Clinical Data Management, Biostatistics & Medical Writing - Regulatory and Lifecycle Safety standalone services The Role The position will be focused on supporting the Sales Enablement function
Uita-te mai târziu13.05.2024 | Full-time | Organonregulations and/or ICH Guidelines regarding in-line medical assessment to ensure regulatory compliance for individual case safety ides in-line medical assessment of individual case safety reports in the context of the available safety data and the known safety profile toassess expectedness
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