01.06.2024 | Full-time | PharmiwebIn accordance with regulatory requirements, i.e., Good Clinical Practice and International Conference on Harmonization guidelines Managing progress by tracking regulatory submissions, recruitment, case report form completion, and data query resolutions Collaborating with experts at study sites and with client
Uita-te mai târziu01.06.2024 | 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 târziu01.06.2024 | 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 târziu01.06.2024 | Full-time | PSIOr equivalent (e.g. Clinical Trial Manager, Clinical Study Team Lead, etc.)Global or regional clinical project management experience, including management of all project services from startup to closureTherapeutic experience in oncology, and/or MS, IBD, hemophilia, other rare disease, infectious diseases
Uita-te mai târziu01.06.2024 | Full-time | WebuildHe/she will be responsible for During the bid study phase and/or new initiative phase, supervising the activities to support the Bidding & Engineering Department, relating to the organization of the P&E structures of the Project, and the possible optimization of the Plants and Machinery needed
Uita-te mai târziu01.06.2024 | Full-time | MAI Fortrea Development LimitedImpacting the development of innovative therapies and treatments. Supported by a diverse team of research professionals, you will collaborate closely with study teams, medical experts, and project managers to ensure the highest quality scientific research and statistical
Uita-te mai târziu