Regulatory and Data Coordinator I
Competitive
HealthcareFull-time
Redmond, WAHealthcarePosted 21d ago
Responsibilities **Regulatory Expertise**: Serve as the subject matter expert for regulatory aspects of clinical study conduct **Study Activation:**Manage the preparation, submission, and tracking of SIPs for clinical studies. Collect essential regulatory documents, prepare and submit documents to the IRB for approval prior to study initiation, set up study in clinical trial management system, and partner with clinic