06.06.2024 | Full-time | PharmiwebDedicated one where you will work exclusively on one sponsors trials and SOPs. Responsibilities Responsible for the leadership of their assigned CRAs on a given study(s), driving the team to ensure study deliverables are met with efficiency and quality Responsible for training the CRAs on the study
Uita-te mai târziu06.06.2024 | 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 târziu06.06.2024 | Full-time | Jucu | BoschIn regards to raw material topics and as per purchasing processesCoordination of sorting activities and inter-disciplinary teamsPermanent cooperation/contact with the suppliers* Position also open for CljP associates willing to develop cross-functional in PQA departmentQualificationsDegree in technical study
Uita-te mai târziu06.06.2024 | Full-time | Cluj-Napoca | AG PrimeRemote and on-site options; Attractive salary and on project bonuses; Possibility to learn advanced software development methodologies; Opportunity for professional development in a young and dynamic environment; Training on the job and possibility to study; Participation in national and international
Uita-te mai târziu06.06.2024 | Full-time | PwCQualificationsDegree Preferred Bachelor DegreePreferred Fields of Study Information TechnologyCertification(s) Preferred Project Management Certification, ITIL Foundation CertificationPreferred Knowledge/SkillsDemonstrates intimate abilities and/or a proven record of success as a team leader in the following areas
Uita-te mai târziu06.06.2024 | 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 târziu06.06.2024 | 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 târziu06.06.2024 | Full-time | 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
Uita-te mai târziu06.06.2024 | Full-time | PharmiwebJob Overview The 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
Uita-te mai târziu06.06.2024 | Full-time | PharmiwebOf the trial (investigator meetings, site visits, quality communication, etc.). Drive study compliance by executing activities within site initiation and start-up, site monitoring, site management and site/study close-out according to internal SOPs and policies. Ensures site staff is trained
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