IQVIA Biotech is seeking a Site Contracts Administrator located in Argentina who has experience working within a CRO.

KNOWLEDGE, SKILLS & ABILITIES:

• Strong written and verbal communication skills.
• Excellent organizational and interpersonal skills.
• Positive attitude and ability to interact with all levels of staff.
• Ability to manage multiple priorities.
• Ability to use sound judgment and assess and recommend specific solutions.
• Ability to work somewhat independently, prioritize effectively and work within a matrix team environment.
• Working knowledge of Word, Excel and Power Point.

• Prepares and delivers investigator / institution research-related agreements to sites. Including but not limited to Clinical Trial Agreements, Budgets, Supplemental Agreements, Amendments, etc.
• Corresponds with investigator sites to obtain contract and budget status updates.
• Updates and maintains study trackers with site statuses and activities.
• Supports the Site Contracts Associates with template population, distribution, site follow up, finalization and tracking of studies.
• Assists Site Contracts Management with study or departmental reports, as needed.
• Follow instructions given by Site Contracts Associate and Site Contracts Management Team.
• Updates study and departmental databases.
• Saves finalized contracts into the appropriate study and departmental folders.
• Conducts all activities according to appropriate IQVIA Biotech and/or sponsor SOPs.
• Performs other duties as required.