27.04.2024 | Full-time | PfizerThe clinical studies. Your project management skills will be leveraged for planning, directing, creating and communicating timelines. You will ensure that the clinical studies are within time, budget and a Manager, you provide guidance to operational teams for managing projects. Your planning skills
Uita-te mai târziu29.04.2024 | Full-time | IQVIASite Manager Study Start-UpReal-World EvidenceEMEA basedJoin us on our exciting journey!IQVIA Real-World Evidence (RWE) teams work with clients to help them collect and use real-world data to generate evidence to meet the needs of regulators, payers, providers, and approach is unique
Uita-te mai târziu02.05.2024 | 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 târziu02.05.2024 | Full-time | Precision Medicine GroupAnd oversee all clinical aspects of your study across multiple countries, ensuring timeline adherence and scope, whilst ensuring quality delivery. We encourage high-energy, dedicated professionals who enjoy a challenge, thrive in the details and flourish in dynamic environments to explore this opportunity. We
Uita-te mai târziu02.05.2024 | Full-time | Société Générale AssurancesWill be required toDaily support tasks (90%)• Technical and functional support of the production;• Monitoring and request - Incident management;• Pick-up calls on a shared hotline;• Features explanations;• Knowledge transfer for new joiners and users;• Crisis management if ase management (5%)• Study
Uita-te mai târziu01.05.2024 | Full-time | SySS GmbHOf study, or comparable vocational training You are creative in finding solutions You are an "around-the-corner thinker" You are enthusiastic about operating systems (Linux), networks
Uita-te mai târziu01.05.2024 | Full-time | IQVIAThe lifecycle of projects. The SES PL will also serve as internal consultants to the IQVIA study team and/or sponsor, present progress, and updates to sponsor, and manage overall delivery of our services on a project, including managing the Site Enablement project budget. Key ResponsibilitiesCollaborate
Uita-te mai târziu01.05.2024 | Full-time | AllucentRemote). As a Sr. Clinical Trial Associate Contractor at Allucent, you act as the primary administrative support to Allucent clinical study teams at Country/Site level, support Clinical Trial Operations and Sponsors, and ensure that the clinical trial is conducted in accordance with regulatory
Uita-te mai târziu01.05.2024 | Full-time | PharmiwebDescription Central Monitor ( Remote Monitor/Risk-Based Monitor) - Romania Sponsor Dedicated The purpose of the Remote 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
Uita-te mai târziu01.05.2024 | Full-time | Craiova | PharmiwebYou’ll do Leverage your expertise. Conduct qualification visits (QV), site initiation visits (SIV), monitoring visits (MV) and termination visits (TV) at assigned clinical sites and generate visit/contact reports. Build relationships. Oversee integrity of the study and utilize problem-solving skills
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