03.06.2024 | Full-time | PharmiwebFor clinical studies across various phases, ensuring adherence to applicable regulations and principles of ICH-GCP. Responsibilities Travel to sites to carry out site selection, initiation, monitoring and close-outs. Support the development of a subject recruitment plan. Evaluate the quality and integrity
Uita-te mai târziu03.06.2024 | Full-time | Craiova | PharmiwebIs a client dedicated one where you will be monitoring studies in such therapeutic areas as immunology, pulmonology, oncology, cardiovascular or neroscience. The CRA is responsible for the initiation, monitoring and closure of assigned sites in clinical studies, in compliance with sponsor's procedural
Uita-te mai târziu03.06.2024 | Full-time | PharmiwebEmerging risk so that the appropriate follow-up action can be taken. Arm the primary site monitor with important information that will enable Sponsor to be the clinical partner of choice; allowing monitors to work differently with site staff and have more productive discussions with our Investigator
Uita-te mai târziu03.06.2024 | Full-time | PharmiwebUnderstanding of the issue /emerging risk so that the appropriate follow-up action can be taken. Arm the primary site monitor with important information that will enable sponsor to be the clinical partner of choice; allowing monitors to work differently with site staff and have more productive discussions
Uita-te mai târziu03.06.2024 | Full-time | Craiova | PharmiwebRelated problems and prioritize workload for self and team You have previous clinical research monitoring experience (including pre-study, initiation, routine monitoring and closeout visits). Fluent Romanian and English Fortrea is actively seeking motivated problem-solvers and creative thinkers who share
Uita-te mai târziu03.06.2024 | Full-time | Cluj-Napoca | PharmiwebEmerging risk so that the appropriate follow-up action can be taken. Arm the primary site monitor with important information that will enable Sponsor to be the clinical partner of choice; allowing monitors to work differently with site staff and have more productive discussions with our Investigator
Uita-te mai târziu03.06.2024 | 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 târziu03.06.2024 | Full-time | PharmiwebFor clinical studies across various phases, ensuring adherence to applicable regulations and principles of ICH-GCP. Responsibilities Travel to sites to carry out site selection, initiation, monitoring and close-outs. Support the development of a subject recruitment plan. Evaluate the quality and integrity
Uita-te mai târziu03.06.2024 | Full-time | PharmiwebFor clinical studies across various phases, ensuring adherence to applicable regulations and principles of ICH-GCP. Responsibilities Travel to sites to carry out site selection, initiation, monitoring and close-outs. Support the development of a subject recruitment plan. Evaluate the quality and integrity
Uita-te mai târziu03.06.2024 | 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
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