06.06.2024 | 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 | 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 | 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 | 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 târziu05.06.2024 | Full-time | E-INFRAProcedure and reports. Lead process and equipment optimization studies. Ensure implementation plan is executed for the system under study and propagated to other applicable systems. Initiate process safety relief audit studies. Independently perform process and project activities with general instruction
Uita-te mai târziu05.06.2024 | 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 târziu05.06.2024 | 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 târziu05.06.2024 | 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 târziu05.06.2024 | Full-time | ParexelWill needIdeally Educated to at least Bachelor of Science level or Bachelor of Science in Nursing or Masters, MD, PhDRelevant clinical research experience in management of international clinical trialsPrior project leadership, or site-based study coordination experienceDemonstrated expertise of feasibility
Uita-te mai târziu05.06.2024 | Full-time | Bacău | Prysmian GroupToolsDesirable technical Knowledge SAP S4/HANA and ECC 6.0Knowledge of other SAP modules (APO, SD, MM, QM, PM, BW)BenefitsKinder GardenMeal ticketsVacation ticketsPrivate insuranceAdditional SkillsGeneral and specific Data Modeling capabilitiesResearch and self study attitudeForward thinking and strategic
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