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Pasantía Country Site Activation - Argentina

Part time, morning, Hybrid - 4 days OB - 1 day HB

Essential Functions:

•    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 Local Teams and other departments as necessary. 
•    Review documents for completeness, consistency and accuracy, under guidance of senior staff.
•    Prepare site regulatory documents, coordinating shipments, distribution and recollection to and from Investigator Sites and Regulatory Bodies. 
•    Distribute completed documents to 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.
•    Support External Commerce Team in the distribution, recollection and tracking of imported and exported materials.

Qualifications
• On course Bachelor´s degree in life science
• Good command of English language
• Evidence of effective problem – solving, analytical, and critical thinking skills.
• Proficiency in alignment with the desired role placement
• Evidence of strong team work and communication skills.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com