Site Activation Coordinator
Core
Coordinate regulatory submissions and document preparation for ethics and competent authorities within the clinical research lifecycle.
Role type
Regulatory Submissions Coordinator
Builds
Regulatory submission packages for clinical trials
Domain
Clinical research / Biotechnology / Pharmaceuticals
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work
Required skills
Regulatory submission experience, document collection, quality control, deadline management, compliance knowledge
Preferred skills
Life Sciences degree, organizational skills, Microsoft Office proficiency
Technologies
Microsoft Office
Responsibilities
Collect vital documents for ethics submissions, prepare study documents for competent authorities, support managers and start-up teams on deadlines, conduct quality control of documents, provide compliance guidance to team members
Seniority
Junior to Mid-level, mentored IC
