03.06.2024 | Full-time | Craiova | 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 târziu03.06.2024 | 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 târziu03.06.2024 | Full-time | Cluj-Napoca | 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 târziu03.06.2024 | Full-time | Cluj-Napoca | 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 târziu03.06.2024 | Full-time | Craiova | 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 târziu03.06.2024 | Full-time | Oradea | 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 târziu03.06.2024 | Full-time | Craiova | 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 târziu03.06.2024 | Full-time | Craiova | 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 târziu03.06.2024 | Full-time | Oradea | 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 târziu03.06.2024 | Full-time | Oradea | 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
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