of protocol/consent documents for ethics/IRB approval. Pre study/placement and initiation visits. Conduct regular monitoring... generated queries in a timely manner. Ensure the satisfactory closeout of investigator sites. Participate, if requested...
, site selection, and potentially co-monitoring, management of Investigator/study site interactions, etc.), review Clinical... (PMDA) is a plus, as is experience of submitting studies to and interacting with Ethics Committees" Experience in early...
proactive issue resolution and maintain trial quality. Manage ethics committee submissions, amendments, and periodic regulatory...) and investigator training. Ensure proper trial documentation, monitor data integrity, and support study closeout. Qualifications...
proactive issue resolution and maintain trial quality. Manage ethics committee submissions, amendments, and periodic regulatory...) and investigator training. Ensure proper trial documentation, monitor data integrity, and support study closeout. Qualifications...
liaison to investigators interested in developing and performing investigator-initiated research Be the primary onboarding... highest standards of ethics and integrity. Good enough is never enough “Good enough” is never enough for the patients...