07.06.2024 | Full-time | MorningstarWith data recording (focus on clearer data) have it done in time & maintain a higher data quality;Integrated data for top-line reporting and invoicing;Compile and analyses sales data (revenue included);Closely studying and analyzing past sales data to determine trends in productivity;Prepare accurate
Uita-te mai târziu07.06.2024 | Full-time | ParexelIndividual and team commitment to quality.- Owns the client relationship at a study level and responsible for client communication ensuring high client ge the project according to budget with revenue recognition and forecasting, including resource management, pass-through management (review
Uita-te mai târziu07.06.2024 | Full-time | Friedrich Lütze GmbHEngineering or a comparable field of study Experience in the development of embedded systems and extensive knowledge of Linux platforms Expertise in the implementation of security standards Experience in identifying and fixing security vulnerabilities of Linux-based systems Programming skills in C/C
Uita-te mai târziu07.06.2024 | Full-time | IQVIAAnd/or review technical and administrative documentation to support business development and enable study initiation and maintenance, as ide specialist regulatory and technical scientific support to facilitate efficient business development, initiation and maintenance of clinical trials, whilst
Uita-te mai târziu07.06.2024 | 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 târziu07.06.2024 | Full-time | Precision Medicine GroupPosition SummaryThe Senior Clinical Data Manager is responsible and manages all aspects of the clinical trial data management process from study start up to post database lock for assigned projects. Standard Operating Procedures - Work Instructions (SOPs/WIs); regulatory directives; study specific
Uita-te mai târziu07.06.2024 | Full-time | ProclinicalThe regulatory team in the preparation of study submissions. The successful candidate will also be involved in feasibility research and will be a key liaison for in-house support onsibilities- Direct and report Site Selection Visits (SSV), Site Initiation Visits (SIV), Routine Monitoring Visits
Uita-te mai târziu07.06.2024 | Full-time | Premier ResearchYou’ll be doing Ensures personal utilization targets and study performance metrics are metActs as primary point of contact for project teams, Sponsors, auditors and other external third parties on assigned studies/programsSupervises department team on assigned studies/programs as neededEnsures
Uita-te mai târziu07.06.2024 | Full-time | IpsosNecessary to provide answers to the objectives of the study. Performs and reviews/provides support in carrying out complex analyzes, in order to obtain information with added value in research reports. Supports presentations of research results to the client. Reviews presentations made by team members
Uita-te mai târziu06.06.2024 | Full-time | MAI Fortrea Development LimitedAre central to the successful delivery of complex oncology projects for a renowned, innovative and global top pharmaceutical company. Our sponsor is looking for Lead Statistical Programmers capable of overseeing studies from the Pharma side. You will be involved in liaising with the entire study team
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