25.05.2024 | Full-time | ProclinicalProclinical is actively looking for a dynamic and detail-oriented Clinical Research Associate II - Senior Clinical Research Associate. This role will mainly focus on conducting various types of onsite monitoring visits and reporting them. As well as managing site communication and supporting
Uita-te mai târziu25.05.2024 | Full-time | Thermo Fisher ScientificAnd internal/external stakeholdersWorking on project work and initiatives for process improvement as required RequirementsEducation and ExperienceDegree in pharmacy, life science or related field0 - 1 years’ clinical monitoring experienceFluency in English and RomanianKnowledge, Skills
Uita-te mai târziu25.05.2024 | Full-time | ParexelDevelopment appeal to you, Parexel could be your next you’ll doLeverage 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 d relationships. Oversee
Uita-te mai târziu25.05.2024 | Full-time | Sowelo Consulting sp. z o.o. sp. k.Services for individuals with a range of conditions Monitor, assess, and adjust interventions to gauge progress and ensure their efficacy Providing therapy outside of clinic (traveling to patient's home or to other locations) Contribute insights to a comprehensive interdisciplinary evaluation, treatment
Uita-te mai târziu25.05.2024 | Full-time | PSIJob DescriptionAs a Clinical Research Associate II at PSI you will enjoy a variety of monitoring tasks and work on clinical studies in different therapeutic indications, maintaining the highest quality standards in the willConduct and report SSV, SIV, RMV, COV onsite monitoring
Uita-te mai târziu25.05.2024 | Full-time | IQVIAAppraising performance and guiding professional development,Rewarding and disciplining employees,Addressing employee relations issues and resolving ificationKnowledge/Qualification in CDISC/CDASH as well as SAS, C+, XML, Python. Bachelor’s degree, or educational equivalence, in clinical
Uita-te mai târziu25.05.2024 | Full-time | CluePointsPlanning and operational monitoring and utilise advanced statistical algorithms to determine the quality of clinical trial data both during and following study execution. We are looking for a new Front-End Software Engineer to join CluePoints! If you are looking for a challenging work experience within
Uita-te mai târziu25.05.2024 | Full-time | CluePointsPlanning and operational monitoring and utilise advanced statistical algorithms to determine the quality of clinical trial data both during and following study execution. We are looking for a new Front-End Software Engineer to join CluePoints! If you are looking for a challenging work experience within
Uita-te mai târziu25.05.2024 | Full-time | ParexelDevelopment appeal to you, Parexel could be your next you’ll doLeverage 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 d relationships. Oversee
Uita-te mai târziu24.05.2024 | Full-time | Thermo Fisher ScientificLaboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on - now and in the a CRA you will perform and coordinate different aspects of the clinical monitoring and site
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