with protocols and regulatory requirements. Maintain and organize clinical trial documentation, including study files, essential... documents, and regulatory submissions. Support the preparation of study-related materials, such as informed consent forms...
Job Overview Perform monitoring and site management work to ensure that sites are conducting the study(ies...) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements...
, and more. With our next generation of subsea vehicles, such as the Libertyâ„¢ E-ROV and Freedomâ„¢ AUV, we push the boundaries of autonomy and remote work... Gulf of Mexico and other remote global locations. Ability to travel domestically and overseas as assigned. Duties...
. When you work at SSOE, you work with the best and you're a part of something bigger than yourself. And providing the... as directed by project leadership. Maintains knowledge of Vantagepoint features, updates, and best practices through self-study...
. You will contribute to the success of clinical trials by ensuring data integrity, participant safety, and compliance throughout the study... lifecycle. What You Will Be Doing: Monitoring clinical trial sites to ensure adherence to study protocols, regulatory...
and site staff to facilitate smooth study conduct. Performing data review and resolution of queries to maintain high...-quality clinical data. Contributing to the preparation and review of study documentation, including protocols and clinical...
selection process. Location and Work Mode Cancún, Q.R., Mexico. Hybrid Remote Who we are Food waste is a $1 trillion... and this article in Forbes. Other recent accolades saw Winnow listed in the 2025 Sunday Times Best Places to Work - a recognition...
studies interfacing with suppliers and Ford cross-functional teams Review supplier incremental tooling work plans compliance... with the GCP study requirements Drive Supplier Process capacity issues resolution as needed - Production constraint risk...
Effective Study Oversight: Develop monitoring plans and tools, ensuring effective study oversight. Optimizing Performance...: Train and mentor Clinical Research Associates (CRAs) to optimize their performance. Timely Study Start-Up & Enrollment...
safety, and operational efficiency. As an Advanced Analytical Monitor, you will work across multiple mid to high-complexity... of experience within the Pharmaceutical, Biotech, or CRO industry. Strong understanding of clinical trial operations, study...