Ethics Submission Specialist (Clinical Research) – Remote
Core
Coordinate ethics and governance submissions for clinical trial study start-up to ensure timely approval and implementation.
Role type
Administrative specialist for clinical research ethics submissions
Builds
Ethics approval packages for clinical trials
Domain
Clinical research / Healthcare administration
Deliverable
client delivery
Required skills
project management, medical terminology knowledge, attention to detail, time management, document review
Preferred skills
experience coordinating human research ethics applications, tertiary qualification in Health or Life Sciences
Responsibilities
Prioritize tasks and balance competing deadlines, convey and interpret complex medical information to various audiences, ensure compliance with ethics and governance requirements (ICH-GCP), lead review and management of detailed scientific documents, monitor status and progression of concurrent submissions
