05.06.2024 | Full-time | Everest Clinical Research Services IncDrive continued success in this exciting clinical research field, we are seeking a committed, skilled, and customer-focused individual to join our winning team as a Clinical Trials IWRS Monitor for our August Research location in Bucharest, Romania with opportunities to work remotely in accordance
Uita-te mai târziu05.06.2024 | Full-time | PharmiwebICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. ICON Romania are currently recruiting
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 târziu05.06.2024 | Full-time | IQVIAEstablish and agree on project planning and project timelines. Ensure monitoring measures are in place and implement contingency plan as rm team members of completion of regulatory and contractual documents for individual ew, track and follow up the progress, the approval and execution
Uita-te mai târziu05.06.2024 | Full-time | Aspen MedicalAspen Medical seeks expressions of interest from experienced and qualified midwife nurses to join our team in supporting an oil and gas project in Libya. As a midwife nurse, you will be responsible for providing high-quality healthcare services in hospital or clinical settings. Contract Details
Uita-te mai târziu05.06.2024 | 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 târziu05.06.2024 | Full-time | PharmiwebICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. ICON Romania are currently recruiting
Uita-te mai târziu05.06.2024 | 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 târziu05.06.2024 | 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 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
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