28.06.2024 | Full-time | IQVIAInitiation, monitoring and close-out visitsSupporting the development of a subject recruitment planEvaluating the quality and integrity of site practices in accordance with regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelinesManaging
Uita-te mai târziu28.06.2024 | Full-time | IQVIAParticipants like ECG, BPM, Glucose Monitoring etc. This role will be responsible for business requirement understanding review, test case authoring and UAT executionResponsible for creating site and subject facing documentation like Investigator Manuals, Patient Facing Guides, Site reference guidesResponsible
Uita-te mai târziu28.06.2024 | Full-time | CPS Fortrea Clinical Development Limited, Maidenhead Sucursala BucurestiFor self and teamYou have previous clinical research monitoring experience (including pre-study, initiation, routine monitoring and closeout visits).Fluent Romanian and EnglishFortrea is actively seeking motivated problem-solvers and creative thinkers who share our passion for overcoming barriers
Uita-te mai târziu28.06.2024 | Full-time | Antal InternationalAnd fields. Through the excellence of their products, they are dedicated to improving patient outcomes and optimizing clinical efficiency. Role We are looking for 1-2 dynamic and results-oriented professionals to join sales team in Romania. The main responsibility will be promoting and selling the portfolio
Uita-te mai târziu28.06.2024 | Full-time | IQVIASelection within assigned country(ies)Contribute and develop to program,/study-specific materials - e.g., monitoring plan, study specific training untable for site-level goal setting and study-specific deliverables for clinical sites within their country(ies)Contribute to, deliver and/or lead
Uita-te mai târziu28.06.2024 | Full-time | Worldwide Clinical TrialsAnd implement them with quality and excellence. We are Worldwide Clinical Trials, and we are a global team of almost 3,000 experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs - in the best possible way. Our mission is to work with passion and purpose
Uita-te mai târziu28.06.2024 | Full-time | PSIJob DescriptionAs a Senior CRA, you will work on the frontline of communication with project stakeholders, ensuring timelines, targets and standards of clinical research projects in a variety of therapeutic indications. You will build and maintain relationships with clinical sites and investigators
Uita-te mai târziu28.06.2024 | Full-time | IQVIAUnderstanding 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 târziu28.06.2024 | Full-time | IQVIAFor clinical trials by serving as Medical Monitor for studies conducted by IQVIA Biotech Clinical on behalf of sponsor companies. The principal function of a Medical Monitor is to serve as primary contact for the sponsor medical team and to serve as front line medical resource to support the project team
Uita-te mai târziu28.06.2024 | Full-time | IQVIAFor completeness and re accurate completion and maintenance of internal systems, databases and tracking tools with project specific ew and provide feedback to management on site performance ew, establish and agree on project planning and project timelines. Ensure monitoring
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