Vaga de Site Activation Coordinator in Argentina
1 vaga: | Publicada em 25/04
- A Combinar
Sobre a vaga
" Under general supervision, perform site activation activities in assigned
studies for investigative sites, according to applicable regulations, SOPs and
work instructions, working closely with the Site Activation Manager (SAM), Project
Management team, and other departments as necessary. Review documents for
completeness, consistency and accuracy, under guidance of senior staff.
" Prepare site regulatory documents, reviewing for completeness and accuracy.
" Inform team members of completion of regulatory and contractual documents for
individual sites.
" Distribute completed documents to sites and internal project team members.
" Support the updating and maintenance of internal systems, databases, tracking
tools, timelines and project plans with accurate and complete project specific
information.
" Review, track and follow up the progress, the approval and execution of
documents, regulatory, ethics, Informed Consent Form (ICF) and Investigator Pack
(IP) release documents.
Qualifications
" Bachelor's Degree in Life sciences or a related field.
" 1 years experience in a healthcare environment.
" Native level of Portuguese + Advanced level of English + Advanced level of
Spanish.
" Good interpersonal communication and organizational skills.
#LI-NRJ #LI-Hybrid
IQVIA is a leading global provider of advanced analytics, technology solutions and
clinical research services to the life sciences industry. We believe in pushing
the boundaries of human science and data science to make the biggest impact
possible to help our customers create a healthier world. Learn more at
https://jobs.iqvia.com