Clinical Trials Regulatory Specialist 1
Competitive
HealthcareFull-time
Stanford, CAScience & PharmaceuticalPosted 19d ago
Responsibilities Independently develop, draft and compile research protocol documents and all materials required for regulatory submissions in compliance with University and external policies Manage and oversee new study initiation process, including educating study staff and sponsors, resolving issues and providing regulatory guidance and support Facilitate and participate in committee meetings, ensure procedures ar