IQVIA
SiteActivationSpecialist
“Site Activation Specialist at IQVIA. Skills: Site Activation, Regulatory, Start Up. Execute feasibility, site identification regulatory, start-up, and maintenance activities. Prepare and manage site reviews”
What They're Looking For.
Must Have
1 - 3 years’ clinical research experience in the Site Activation/Regulatory and Start Up team in a CRO supporting maintainance protocols, Bachelor's Degree Life sciences or a related field, Advanced level of English skills
What You'll Do.
site identification regulatory
and maintenance activities
Prepare and manage site reviews
Negotiate site documents and contracts
and report on site performance
Serve as the primary point of contact for investigative tracks completion
Ensure contracts are fully executed
Establish project timelines
Serve a Single Point of Contact (SPOC)
site activation and some maintenance activities
Review documents for completeness
consistency and accuracy
Prepare site documents
reviewing for completeness and accuracy
Inform team members of completion of regulatory contractual
Distribute completed documents to sites and internal project team members
Update and maintain internal systems
timelines and project plans
track and follow up the progress
the approval and execution of required documents
How You'll Work.
Team & Collaboration
working closely with the Site Activation Manager (SAM); Project Management team; other departments as necessary; Inform team members of completion of regulatory contractual; Distribute completed documents to sites and internal project team members
Communication Scope
Great communication skills
Process & Methodology
Establish project timelines, Update and maintain project plans
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