Clinical Study and Regulatory Assistant
Core
Support the Cancer Genomics Program by managing regulatory submissions, curating clinical data into eCRFs, and ensuring compliance with research protocols.
Role type
Clinical Study and Regulatory Assistant
Builds
Genomics clinical trials and research studies
Domain
Oncology / Clinical Research / Genomics
Deliverable
client delivery
Required skills
Regulatory compliance, clinical data curation, eCRF management, medical terminology, Microsoft Excel proficiency, administrative coordination
Preferred skills
Clinical research experience, oncology knowledge, regulatory issues knowledge, Clinical Research Professional certification
Technologies
Microsoft Excel, electronic case report forms (eCRFs)
Responsibilities
Prepare REB and CAPCR submissions, create and review study documents, curate clinical data from source documents, collect consent forms, interpret regulations and protocols, attend study meetings, perform administrative tasks
Seniority
Entry-level to Junior