06.06.2024 | 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 | 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 | ContinentalOn the respective you will be doingMarket study on specific electronic components;Keeping up with new available technology and opportunities;Keep close contact with AP (Advanced Purchasing);Support colleagues with knowledge with regards to available components in company specific database;Support
Uita-te mai târziu06.06.2024 | Full-time | HoneywellSales team spread over different countriesBuild and register Engineer To Order application and study work to keep available for the EMEA salesNetwork in different HTS engineering hubs in EMEA and worldwideSupport Internal Sales Support Bucharest team technicallySkills/Qualifications Bachelor or Master
Uita-te mai târziu05.06.2024 | Full-time | De Micco & Friends LAWYERSCivil and crime law. (Established lawyer teams may also apply). You are at least in your mid 30s and have already been successful at a law firm or as an independent lawyer or auditor. In addition, you ideally meet the following criteria Relevant major field of study relating to commercial, civil
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 târziu04.06.2024 | Full-time | Bacău | Prysmian GroupOn” approach, working in a dynamic and fast paced environment Additional SkillsProject Management SkillsResearch and self study attitudeGood written and oral communication skillsCloud transformation project Benefits- Kinder Garden- Meal tickets- Vacation tickets- Private insuranceClosure of the postingYour
Uita-te mai târziu04.06.2024 | Full-time | Cluj-Napoca | Human DirectRelated incident response, especially when pertaining to data integrity Areas of Experience React Development Tools HTML CSS JavaScript - SQL Test-Driven Workflow (TDD) Git - GitHub Requirements Requirements B.S. in Computer Science or related area of study. 8+ years in progressive, hands
Uita-te mai târziu03.06.2024 | Full-time | PSIJob DescriptionThe Milestone One Site Coordinator role supports Clinical Study Sites in clinical trial related activities according to ICH-GCP, local regulations, protocol requirements within Study specific defined timelines and enrollment function of the role may include, but not limited
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