06.06.2024 | Full-time | Cluj-Napoca | ARRK Research & Development SRLBe a graduate engineer in applied mathematics, physics, mechanical engineering, or you must have had a comparable education;During or after your course of study, you will have to have developed an interest in technical calculation - structural mechanics, and ideally you bring along some practical working
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 | 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 | 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 | PharmiwebOf clinical trials at a country level in accordance with ICH-GCP and other applicable local regulations. RESPONSIBILITIES OVERVIEW Partner with global, local country teams and study team to provide high level country strategy, drive study progress and country level study delivery. (Accountable for study
Uita-te mai târziu06.06.2024 | Full-time | Oradea | 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 | PharmiwebIn Romania . Responsibilities include All details of site management as prescribed in the project plans Recruitment of potential investigators, preparation of EC submissions, notifications to regulatory authorities, translation of study-related documentation, organization of meetings and other tasks
Uita-te mai târziu06.06.2024 | Full-time | Craiova | 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 | Craiova | PharmiwebIn Romania . Responsibilities include All details of site management as prescribed in the project plans Recruitment of potential investigators, preparation of EC submissions, notifications to regulatory authorities, translation of study-related documentation, organization of meetings and other tasks
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 târziu