to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used... partner for the pharmaceutical industry in the development and manufacturing of new treatments for patients worldwide...
support and assistance for the University of Cincinnati Cancer Center Clinical Trials Office (CTO). Duties can span a broad... established CTO workflows and CTO/UC Health standard operating procedures. Consent participants to interventional clinical trials...
and manufacturing support teams Work with clinical affairs on various aspects of clinical trials and clinical reports... Quality Systems standards and clinical investigations Experience working directly with FDA, notified bodies...
Conduct) requirements for clinical trials and other Medical Affairs activities; thorough knowledge of FDA regulations..., ICH guidelines and GCPs governing the conduct of clinical trials Must be able to work with autonomy and independence...
diversity in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity... partners in the Worldwide Commercialization Excellence (WCE) organization to understand strategic business objectives, develop...
About the Role: Culmen International is seeking a Clinical Protocol Developer to work on site in Portsmouth, VA... of investigator-initiated trials to include coordination of the protocol submission, submission of amendments and regulatory...
trials worldwide. As part of our team, you’ll be instrumental in helping us achieve our mission of improving patient lives..., we invite you to apply for this exciting opportunity at Signant Health. Join us in our mission to revolutionize clinical trials...
trials worldwide. As part of our team, you’ll be instrumental in helping us achieve our mission of improving patient lives..., we invite you to apply for this exciting opportunity at Signant Health. Join us in our mission to revolutionize clinical trials...
Conduct) requirements for clinical trials and other Medical Affairs activities; thorough knowledge of FDA regulations..., ICH guidelines and GCPs governing the conduct of clinical trials Must be able to work with autonomy and independence...
of clinical evidence for pre-market trials/studies as it applies to product lifecycle. Studies must be scientifically valid, meet... required and a minimum of 5 years of experience managing/leading clinical studies/trials/teams (preferably with people leadership/managerial...