14.05.2024 | Full-time | ParexelResponsibilitiesPartners with study teams, with responsibility management of required regulatory activities, standards and deliverables associated with CTA submission development and completion of relative associated documentation as and attends relevant meetings to advocate
Uita-te mai târziu14.05.2024 | Full-time | Teva PharmaceuticalsE.g., study protocol, IB, informed consent/assent form, clinical study report, integrated summaries of safety, Common Technical Document (CTD) submissions, Regulatory Agency responses, IRB/EC requests, briefing books, DMC charters, Medical Monitoring Plans, Statistical Analysis Plans, and other
Uita-te mai târziu14.05.2024 | Full-time | Cluj-Napoca | Hanwha Q CELLS GmbHOf study In your training or in the last 3 years, you have already acquired valuable practical knowledge in the field of IT support, especially in the topic domain You are now keen to put this to the test in a large, sustainable company You describe yourself as eager to learn and enjoy immersing yourself
Uita-te mai târziu13.05.2024 | Full-time | DellLearn and develop through awareness and study of information security events, techniques, and threat actor TTP’s.Assumes ownership in problem
Uita-te mai târziu13.05.2024 | Full-time | DeloitteTo leverage technology for process improvement. The ideal candidate meets the following requirements Preferred fields of study Accounting, Engineering, Finance, Information Technology, Operations Management/Research 2 to 4 years in consulting companies or market experience equivalent Know some
Uita-te mai târziu13.05.2024 | Full-time | Signant HealthOf the business. The position gives you a great view on how all aspects of technical design activities are performed for a to join the Best Team of Your Life?We’re looking for people who are excited by the potential to make a difference in the world. You don’t need to have a clinical background
Uita-te mai târziu13.05.2024 | Full-time | Precision Medicine GroupAnd works closely with our project teams to provide oversight, strategic expertise in the planning, coordination, and delivery of all activities for designated clinical study projects to ensure that project objectives of quality, scope, cost, and time are ntial functions of the job include
Uita-te mai târziu12.05.2024 | Full-time | Bacău | Prysmian GroupTicketsPrivate insuranceAdditional SkillsGeneral and specific Data Modeling capabilitiesResearch and self study attitudeForward thinking and strategic planningOrganization and
Uita-te mai târziu11.05.2024 | Full-time | IQVIAWith regulatory requirements, i.e., Good Clinical Practice and International Conference on Harmonization guidelinesManaging progress by tracking regulatory submissions, recruitment, case report form completion, and data query resolutionsCollaborating with experts at study sites and with client
Uita-te mai târziu10.05.2024 | Full-time | NATEKIn in Biotechnological sector. Responsibilities Impact Assessment and Configuration changes Analyses - Determine the areas of the system impacted by the study upgrades and define the test scope, scenarios, and test cases accordingly. Analyze the scope of the upgrade and understand the changes made to the system
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