11.06.2024 | Full-time | ParexelFor a studyServe as the primary point of contact internally and with external customers as needed regarding study technology, data integrations, and requirementsCollaborate with Project Leaders, Project Specialists, and other study team members on study technology needs from the point of early trial planning
Uita-te mai târziu11.06.2024 | Full-time | PSIVisitsPerform CRF review, source document verification and query resolutionBe responsible for site communication and managementBe a point of contact for in-house support services and vendorsCommunicate with internal project teams regarding study progressParticipate in feasibility researchSupport regulatory team
Uita-te mai târziu11.06.2024 | Full-time | IQVIAProgress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolutionCollaborating with experts at study sites and with client representativesQualificationsUniversity degree in scientific discipline or health careAt least 2 years of on-site monitoring
Uita-te mai târziu11.06.2024 | Full-time | IQVIANecessaryProvide executive leadership for study teams when necessary to manage project related challenges and to achieve exemplary customer service. Ensure the improvement of the execution of clinical project processesDrive quality or process improvement initiatives related to corporate or departmental strategic
Uita-te mai târziu11.06.2024 | 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 târziu11.06.2024 | 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 târziu11.06.2024 | Full-time | PSI CROAnd investigators. Your focus will be on subjects’ rights, safety and well-being and quality of data compliance. Your responsibilities will include Conducting and reporting all types of onsite monitoring visits Driving the study startup phase (if applicable) Performing CRF reviews, source document verification
Uita-te mai târziu11.06.2024 | Full-time | GfKProject kickoff meetings for all assigned studies to ensure all involved parties understand timelines, responsibilities and study ort research project teams by leveraging relationships with overseas suppliers to facilitate communications, troubleshooting and issue dinate
Uita-te mai târziu11.06.2024 | Full-time | IQVIAIQVIA is looking to appoint statistical programmers to utilize the SAS programming language to develop clinical study report materials according to the objectives of a clinical trial for regulatory submissions. Programming and performing related tasks serving the full spectrum of statistical
Uita-te mai târziu11.06.2024 | Full-time | IQVIAJob OverviewThe purpose of the Central Monitor is to de-risk studies as early as possible by analyzing data at the macro-level for insights that are not visible when monitoring individual data points /study sites-thereby enabling sponsor to take early interventions to mitigate potential risks
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