06.06.2024 | Full-time | IQVIAJob OverviewManage and support the operational elements and execution of studies and/or programs to ensure delivery; time and quality resulting in strong financial performance and customer satisfaction and in accordance with SOPs; policies and practices from pre-award to close-out. Work with study
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
Uita-te mai târziu06.06.2024 | Full-time | PharmiwebWith experts at study sites and with client representatives. Key Skills and Requirements University degree in a scientific discipline or health care. On-site monitoring experience. Good knowledge of clinical research regulatory requirements. Proficiency in MS Office. Excellent command of Romanian and English
Uita-te mai târziu06.06.2024 | Full-time | ContinentalPrograms for platform products after SOP by introduction of new components/technologies(re-design to cost and cost& value analysis).QualificationsCompleted studies (,Dipl.) in economics or engineering or a comparable field of study;Several years of professional experience in purchasing (operational
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 | 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 | Linde Gaz Romania SRLIdentifying sales projects and opportunities Active assistance for the reinforcement of existing partners´ loyalty The management of the bids and direct procurement procedures organized by the contracting institutions You will also develop and streamline the activity of Sleep Study Laboratories Participation
Uita-te mai târziu06.06.2024 | Full-time | ParexelFor the TMF and has advanced knowledge on PAREXEL or Sponsor specific Electronic Trial Master File (eTMF) and paper documents management processes and procedures. Represents a primary Point of Contact for the study TMF and assumes the ability to coordinate study TMF activities with a high degree
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