Iqvia
SiteActivationSpecialist
“Site Activation Specialist at Iqvia. Skills: Site Activation, Regulatory Documents, Document Management. Prepare site regulatory documents. Review regulatory documents for completeness”
What You'll Achieve.
Ensure accuracy, compliance, and timely delivery of Informed Consent Forms
Industry & Context.
Problem-solving skills
What They're Looking For.
Must Have
Bachelor’s in Life Sciences or related field, At least 4+ years’ experience as Site Activation Specialist, Knowledge of ICH/GCP and regulatory requirements
What You'll Do.
Prepare site regulatory documents
Review regulatory documents for completeness
Inform team members of document completion
Distribute completed documents to sites
Support updating internal systems
Track progress of documents
Follow up on document approval
Follow up on document execution
How You'll Work.
Team & Collaboration
Partner with global and country teams; Inform team members of completion; Distribute completed documents to internal project team members
Communication Scope
Communication skills
Process & Methodology
Manage multiple projects
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